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Hydrochloric Acid → Methyl 2-methyl-1H-benzimidazole-5-carboxylate

HRID 1110809
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HRID 1110809 반응식
Cl.[CH3:2][C:3]1[NH:4][C:5]2[CH:11]=[C:10]([C:12]([OH:14])=[O:13])[CH:9]=[CH:8][C:6]=2[N:7]=1.Cl.[CH3:16]O>>[CH3:2][C:3]1[NH:4][C:5]2[CH:11]=[C:10]([C:12]([O:14][CH3:16])=[O:13])[CH:9]=[CH:8][C:6]=2[N:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 313Hydrochloric AcidHCID 887MethanolHCID 173682452-Methyl-1H-benzimidazole-5-carboxylic acid hydrochloride

생성물 1

HCID 14856789Methyl 2-methyl-1H-benzimidazole-5-carboxylate수율 93.2%

실험 절차

Mass spectrum (FAB, Pos): m/z 177 (M+ +1, as a free base). ##STR15## 2-Methylbenzimidazole-5-carboxylic acid hydrochloride, 6.6 g (32.5 mmols), was added to 200 ml of methanol and 5 ml of conc. hydrochloric acid was added to the mixture followed by heating to reflux for 8 hours. The solvent was distilled off under reduced pressure and 200 ml of water was added to the residue. After 1 N sodium hydroxide solution was added to the mixture to adjust pH to 9 to 10, the mixture was extracted with ethyl acetate. The ethyl acetate layer was dried over anhydrous magnesium sulfate and filtered. The solvent was distilled off to give 5.5 g (93.2%) of methyl 2-methyl-benzimidazole-5-carboxylate.

후처리

  1. additionwas added to the mixture
  2. temperatureby heating
  3. temperatureto reflux for 8 hours
  4. distillationThe solvent was distilled off under reduced pressure and 200 ml of water
  5. additionwas added to the residue
  6. additionAfter 1 N sodium hydroxide solution was added to the mixture
  7. extractionthe mixture was extracted with ethyl acetate
  8. dry with materialThe ethyl acetate layer was dried over anhydrous magnesium sulfate
  9. filtrationfiltered
  10. distillationThe solvent was distilled off

출처 및 근거

ORD 기록
ord-9adf109a6694448bb2625f995fc465b7
출처 데이터셋
uspto-grants-1990_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04977175

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