Home Cart 0 Sign in  

[ CAS No. 1338494-62-4 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
Chemical Structure| 1338494-62-4
Chemical Structure| 1338494-62-4
Structure of 1338494-62-4 * Storage: {[proInfo.prStorage]}
Cart0 Add to My Favorites Add to My Favorites Bulk Inquiry Inquiry Add To Cart

Quality Control of [ 1338494-62-4 ]

Related Doc. of [ 1338494-62-4 ]

Alternatived Products of [ 1338494-62-4 ]

Product Details of [ 1338494-62-4 ]

CAS No. :1338494-62-4 MDL No. :MFCD20441336
Formula : C3HF3N2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 154.05 Pubchem ID :-
Synonyms :

Safety of [ 1338494-62-4 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 1338494-62-4 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 1338494-62-4 ]

[ 1338494-62-4 ] Synthesis Path-Downstream   1~3

  • 1
  • [ CAS Unavailable ]
  • [ 1338494-62-4 ]
YieldReaction ConditionsOperation in experiment
With methanesulfonic acid In water 1 example 1 Compound 3 (130.62 g),Pyridine (505.82 g),Trifluoroacetic anhydride (209.78 g)Were reacted at 10 ° C. to obtain a gas of Compound 4.Separately, Compound 1 (40.00 g, 575.6 mmol) and methanol (79.22 g)Was cooled to -10 ° C., 28% sodium methylate / methanol solution (111.16 g) and methanol were added and stirred,Compound 2 was prepared in the system. To the obtained reaction solution, a gas of Compound 4 was introduced at -10 ° C., stirred,Compound 5 was prepared in the system. After raising the temperature to 25 ° C,Dimethyl carbonate (155.68 g),28% sodium methylate / methanol solution (166.62 g) was added,And reacted at 60 ° C. to prepare compound 6 in the system.To the resulting reaction solution were added water (400.05 g),And methanesulfonic acid (110.66 g), And compound 7 was prepared in the system.The mixture was extracted with 4-methyl-2-pentanone (481.25 g), and the aqueous layer and the organic layer were separated.The obtained organic layer was washed with water (400.21 g). The two obtained aqueous layers were successively treated with 4-methyl-2-pentanone (320.11 g). Combining the two organic layers,4-methyl-2-pentanone (32.05 g), imidazole (43.12 g)And methanol (63.32 g) were added.The obtained solution was mixed with 343.72 g. Toluene (970.81 g) was added at 25 ° C., and the obtained solid was collected by filtration to give a crude product(Compound 8).Methanol (949.82 g) was added to the crude product,And methanesulfonic acid (88.25 g) were added, the mixture was concentrated to a liquid amount of 395.80 g, and water (120.51 g) was added. It was extracted with 4-methyl-2-pentanone (481.82 g)The organic layer was washed with water (200.12 g).The two aqueous layers were back-extracted in sequence with 4-methyl-2-pentanone (320.51 g). The two organic layers were combined to give an organic layer containing Compound 7. 4-methyl-2-pentanone (32.11 g), imidazole (33.16 g), and methanol (63.36 g) were added to the obtained organic layer.The resulting solution was concentrated to a liquid volume of 340.75 g. Toluene (970.22 g) was added at 25 ° C. The obtained solid was collected by filtration,Compound 8 (105.03 g, yield 82%)As white crystals.
  • 2
  • [ 288-32-4 ]
  • [ 1338494-62-4 ]
  • [ 2226335-09-5 ]
YieldReaction ConditionsOperation in experiment
105.03 g In methanol; toluene at 25℃; 1 example 1 Compound 3 (130.62 g),Pyridine (505.82 g),Trifluoroacetic anhydride (209.78 g)Were reacted at 10 ° C. to obtain a gas of Compound 4.Separately, Compound 1 (40.00 g, 575.6 mmol) and methanol (79.22 g)Was cooled to -10 ° C., 28% sodium methylate / methanol solution (111.16 g) and methanol were added and stirred,Compound 2 was prepared in the system. To the obtained reaction solution, a gas of Compound 4 was introduced at -10 ° C., stirred,Compound 5 was prepared in the system. After raising the temperature to 25 ° C,Dimethyl carbonate (155.68 g),28% sodium methylate / methanol solution (166.62 g) was added,And reacted at 60 ° C. to prepare compound 6 in the system.To the resulting reaction solution were added water (400.05 g),And methanesulfonic acid (110.66 g), And compound 7 was prepared in the system.The mixture was extracted with 4-methyl-2-pentanone (481.25 g), and the aqueous layer and the organic layer were separated.The obtained organic layer was washed with water (400.21 g). The two obtained aqueous layers were successively treated with 4-methyl-2-pentanone (320.11 g). Combining the two organic layers,4-methyl-2-pentanone (32.05 g), imidazole (43.12 g)And methanol (63.32 g) were added.The obtained solution was mixed with 343.72 g. Toluene (970.81 g) was added at 25 ° C., and the obtained solid was collected by filtration to give a crude product(Compound 8).Methanol (949.82 g) was added to the crude product,And methanesulfonic acid (88.25 g) were added, the mixture was concentrated to a liquid amount of 395.80 g, and water (120.51 g) was added. It was extracted with 4-methyl-2-pentanone (481.82 g)The organic layer was washed with water (200.12 g).The two aqueous layers were back-extracted in sequence with 4-methyl-2-pentanone (320.51 g). The two organic layers were combined to give an organic layer containing Compound 7. 4-methyl-2-pentanone (32.11 g), imidazole (33.16 g), and methanol (63.36 g) were added to the obtained organic layer.The resulting solution was concentrated to a liquid volume of 340.75 g. Toluene (970.22 g) was added at 25 ° C. The obtained solid was collected by filtration,Compound 8 (105.03 g, yield 82%)As white crystals.
  • 3
  • [ 288-32-4 ]
  • [ 1338494-62-4 ]
  • [ 2226335-11-9 ]
YieldReaction ConditionsOperation in experiment
3.13 g With 4-methyl-morpholine; Isopropyl acetate; N-ethyl-N,N-diisopropylamine; trichlorophosphate at 25 - 40℃; for 5h; 2.2 Second Step Production Method of Compound 9 Compound 7 (3.09 g, 20.1 mmol), isopropyl acetate (14.7 mL), imidazole (1.67 g, 24.5 mmol), N, N- diisopropylethylamine (5.12 g, 39.6 mmol) and N- Methyl morpholine (0.06 g, 0.6 mmol) was mixed at 25 ° C. and phosphorous oxychloride (4.49 g, 29.3 mmol) was added. The reaction solution was heated to 40 ° C. and stirred for 5 hours. The reaction solution was cooled to 25 ° C. and added dropwise to a 25% aqueous dipotassium hydrogen phosphate solution (46.4 mL) at 0 ° C. over 20 minutes for extraction. The extract was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (hexane / ethyl acetate) to obtain compound 9 (3.13 g, 15.3 mmol).
Same Skeleton Products
Historical Records

Related Functional Groups of
[ 1338494-62-4 ]

Alcohols

Chemical Structure| 1456-22-0

[ 1456-22-0 ]

3-Phenyl-1,2,4-oxadiazol-5-ol

Similarity: 0.51

Related Parent Nucleus of
[ 1338494-62-4 ]

Oxadiazoles

Chemical Structure| 51791-12-9

[ 51791-12-9 ]

3-(Chloromethyl)-1,2,4-oxadiazole

Similarity: 0.63

Chemical Structure| 1184986-84-2

[ 1184986-84-2 ]

(5-Methyl-1,2,4-oxadiazol-3-yl)methanamine hydrochloride

Similarity: 0.58

Chemical Structure| 1192-80-9

[ 1192-80-9 ]

3-(Chloromethyl)-5-methyl-1,2,4-oxadiazole

Similarity: 0.55

Chemical Structure| 1456-22-0

[ 1456-22-0 ]

3-Phenyl-1,2,4-oxadiazol-5-ol

Similarity: 0.51