Acetic Acid → Methyl 2-isocyano-2-(2-thienylmethyl)butyrate

HRID 1722734노트

반응식

HRID 1722734 반응식
CC(C)([O-])C.[K+].[N+:7]([CH:9]([CH2:14][CH3:15])[C:10]([O:12][CH3:13])=[O:11])#[C-:8].Br[CH2:17][C:18]1[S:19][CH:20]=[CH:21][CH:22]=1.C(O)(=O)C>O1CCCC1>[N+:7]([C:9]([CH2:17][C:18]1[S:19][CH:20]=[CH:21][CH:22]=1)([CH2:14][CH3:15])[C:10]([O:12][CH3:13])=[O:11])#[C-:8]

참가 물질

6

반응 조건

온도
-30 °C

실험 절차

A suspension of potassium tert.-butoxide (5.5 g) in tetrahydrofuran (50 ml) is cooled to -30° C., and a solution of methyl 2-isocyanobutyrate (5.5 g) in tetrahydrofuran (10 ml) is added dropwise to the suspension at -30° C. The mixture is stirred at the same temperature for 30 minutes and a solution of 2-bromomethylthiophene (6.9 g) in tetrahydrafuran (10 ml) is added dropwise to the mixture. The mixture is stirred at room temperature for 4 hours, adjusted to pH 7 with acetic acid and then concentrated under reduced pressure to remove solvent. The residue is dissolved in a mixture of ethyl acetate and water and the organic layer is collected therefrom. The organic layer is washed with an aqueous saturated sodium chloride solution, dried and concentrated to remove solvent. The residue is distilled under reduced pressure, whereby methyl 2-isocyano-2-(2-thienylmethyl)butyrate (7.7 g) is obtained as pale yellow oil.

후처리

  1. stirringThe mixture is stirred at room temperature for 4 hours
  2. concentrationconcentrated under reduced pressure
  3. customto remove solvent
  4. dissolutionThe residue is dissolved in a mixture of ethyl acetate and water
  5. customthe organic layer is collected
  6. washThe organic layer is washed with an aqueous saturated sodium chloride solution
  7. customdried
  8. concentrationconcentrated
  9. customto remove solvent
  10. distillationThe residue is distilled under reduced pressure

출처 및 근거

ORD 기록
ord-759e756f67714c06833db969e245f1ad
출처 데이터셋
uspto-grants-1989_08
특허 번호
US04857543

반응 노트

불러오는 중…