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Chemical Structure| 431-46-9 Chemical Structure| 431-46-9

Structure of 431-46-9

Chemical Structure| 431-46-9

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Product Details of [ 431-46-9 ]

CAS No. :431-46-9
Formula : C3H5F3O2
M.W : 130.07
SMILES Code : COC(O)C(F)(F)F
MDL No. :MFCD00013572
InChI Key :GWTBCUWZAVMAQV-UHFFFAOYSA-N
Pubchem ID :9892

Safety of [ 431-46-9 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H225-H302
Precautionary Statements:P305+P351+P338
Class:3
UN#:3271
Packing Group:

Application In Synthesis of [ 431-46-9 ]

* 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 [ 431-46-9 ]

[ 431-46-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 61160-18-7 ]
  • [ 431-46-9 ]
  • [ 1064077-32-2 ]
YieldReaction ConditionsOperation in experiment
37.8% With potassium carbonate; at 120℃; for 108h;Product distribution / selectivity; EXAMPLE 19; Preparation of 3-Hydroxy-2-methyl-5-(2,2,2-trifluoro-1-hydroxy-ethyl)-1H-pyridin-4-one; Preparation of 3-Benzyloxy-2-methyl-5-(2,2,2-trifluoro-1-hydroxy-ethyl)-1H-pyridin-4-one; 3-Benzyloxy-2-methyl-1H-pyridin-4-one (1 g, 4.64 mmol) was mixed with potassium carbonate (0.2 g, 1.45 mmol) and CF3CH(OCH3)OH (4.34 g, 33.36 mmol) in sealed parallel synthesizer reactor and heated at 120° C. metal block temperature for 2 days. The mixture was cooled, and an additional amount of potassium carbonate (2 g, 14.5 mmol) and CF3CH(OCH3)OH (2 g, 15.30 mmol) was added. The mixture was again heated in a sealed tube at 120° C. for 60 hours. The mixture was cooled to room temperature and then evaporated to dryness. The residual material was purified by column chromatography (5percent MeOH:dichloromethane) to give 3-benzyloxy-2-methyl-5-(2,2,2-trifluoro-1-hydroxy-ethyl)-1H-pyridin-4-one (0.55 g, 37.8percent yield).H-NMR (300 MHz, DMSO-d6) delta 2.08 (s, 3H, CH3), 5.06 (dd, 2H, CH2Ph, J=11, 8.4 Hz), 5.35 (m, 1H, CHCF3), 7.31-7.35 (m, 5H, Ph), 7.57 (s, 1H, CH).
24% In dichloromethane; for 144h;Heating / reflux;Product distribution / selectivity; B. Preparation of 3-Benzyloxy-2-methyl-5-(2,2,2-trifluoro-1-hydroxy-ethyl)-1H-pyridin-4-one A mixture of <strong>[61160-18-7]3-benzyloxy-2-methyl-1H-pyridin-4-one</strong> (10.0 g, 46.4 mmol), potassium carbonate (19 g, 138 mmol), and CF3CH(OH)OCH3 (35 mL, 0.35 mol) in a 500 mL 3-necked round bottom flask equipped with a mechanical stirrer was heated to reflux for 6 days. The progress of the reaction was monitored by HPLC Method 3 (Example 24). Analysis of the HPLC data indicated that there was about 42percent conversion. The reaction was stopped, and dichloromethane and deionized water were added. The organic fraction was collected, washed with brine, dried over Na2SO4, filtered and concentrated to dryness. Purification of the residue by column chromatography on silica (methanol/dichloromethane 2/100 to 5/100 v:v) afforded 3-benzyloxy-2-methyl-5-(2,2,2-trifluoro-1-hydroxy-ethyl)-1H-pyridin-4-one as a solid product (3.5 g, 24percent yield, HPLC Method 3 (Example 24), RT=14.3 min). 1H NMR (DMSO-d6) 8 ppm: 11.68 (br s, 1H), 7.58 (s, 1H), 7.35, (m, 5H), 5.34 (q, J=7.3 Hz, 1H), 5.06 (m, 2H), 2.08 (s, 3H); MS-ESI (m/z) 313.7 [M+1]+, 206.1, 91.1 (100percent).
 

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