Home Cart 0 Sign in  

[ CAS No. 59769-22-1 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
Chemical Structure| 59769-22-1
Chemical Structure| 59769-22-1
Structure of 59769-22-1 * Storage: {[proInfo.prStorage]}
Cart0 Add to My Favorites Add to My Favorites Bulk Inquiry Inquiry Add To Cart

Quality Control of [ 59769-22-1 ]

Related Doc. of [ 59769-22-1 ]

Alternatived Products of [ 59769-22-1 ]

Product Details of [ 59769-22-1 ]

CAS No. :59769-22-1 MDL No. :MFCD00182122
Formula : C11H11ClN2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 238.67 Pubchem ID :-
Synonyms :

Safety of [ 59769-22-1 ]

Signal Word: Class:
Precautionary Statements: UN#:
Hazard Statements: Packing Group:

Application In Synthesis of [ 59769-22-1 ]

* 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 [ 59769-22-1 ]

[ 59769-22-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 4857-06-1 ]
  • [ 105-36-2 ]
  • [ 59769-22-1 ]
YieldReaction ConditionsOperation in experiment
97% With sodium hydride In paraffin oil 8 4.1.8 Ethyl 2-(2-chloro-1H-benzo[d]imidazol-1-yl)acetate 11 Compound 11 was obtained from commercial 2-chlorobenzimidazole 5 (0.500g, 3.30mmol), sodium hydride suspension (60% suspension in paraffin oil) (0.132g, 3.30mmol) and ethyl bromoacetate (0.38mL, 3.30mmol), according to the procedure described for derivatives 9 and 10. Yield: 97%; m.p.=120-122°C; 1H NMR (DMSO-d6, ppm): 1.23 (t, 3H, J=7.2Hz); 4.20 (q, 2H, J=7.2Hz); 5.27 (s, 2H); 7.26-7.34 (m, 2H); 7.62-7.65 (m, 2H).
93% With triethanolamine at 20℃; for 0.1h; Sonication; Green chemistry;
With sodium hydride In N,N-dimethyl-formamide; mineral oil at 0 - 20℃; 29.A To a solution of 2-chloro-lH-benzo [d] imidazole (10 g) and NaH (60% in oil, 3.15 g) in DMF (150 mL) was added ethyl bromoacetate (11.0 mL) at 0 °C. After stirring overnight at room temperature, the reaction mixture was quenched with water and extracted with AcOEt. The extract was washed with water and brine, dried over MgSO^, and concentrated under reduced pressure. The precipitate was crystallized from AcOEt/hexane to give the title compound (12 g) .MS (ESI+) , found: 239.1.XH NMR (300 MHz, CDC13) δ 1.27 (3H, t, J = 7.2 Hz), 4.25 (2H, q, J = 7.2 Hz), 4.90 (2H, s) , 7.17-7.25 (1H, m) , 7.27-7.35 (2H, m) , 7.67-7.75 (1H, m) .
Same Skeleton Products
Historical Records