Water → Ethyl (1R,2R)-2-(hydroxymethyl)cyclopropanecarboxylate

HRID 1798455

반응식

HRID 1798455 반응식
[CH:1]([CH:3]1[CH2:5][CH:4]1[C:6]([O:8][CH2:9][CH3:10])=[O:7])=[O:2].[BH4-].[Na+].[NH4+].[Cl-].O>CO>[OH:2][CH2:1][C@@H:3]1[CH2:5][C@H:4]1[C:6]([O:8][CH2:9][CH3:10])=[O:7]

참가 물질

6

실험 절차

To a solution of ethyl 2-formyl-1-cyclopropanecarboxylate (1.5 eq.) in methanol (0.7 M) at 0° C. was added sodium borohydride (1.5 eq.) in portions over 30 min. The mixture was allowed to stir at rt for 1.5 h and then cooled in an ice bath. Saturated aqueous NH4Cl solution was added dropwise, and the mixture was stirred for 1.5 h. Water was added, and the aqueous layer was extracted with. The combined organic extracts were washed with brine, dried over MgSO4, and concentrated to afford a racemic mixture of the title compound as a clear oil. Racemic trans 2-(hydroxymethyl)cyclopropanecarboxylate was purified by a Chiral Pak AD preparative column (10% EtOH/Hex) to afford two enantiomers. Ethyl (1R,2R)-2-(hydroxymethyl)cyclopropanecarboxylate was eluted as the faster enantiomer (retention time=12.94 min)

후처리

  1. temperaturecooled in an ice bath
  2. stirringthe mixture was stirred for 1.5 h
  3. extractionthe aqueous layer was extracted with
  4. washThe combined organic extracts were washed with brine
  5. dry with materialdried over MgSO4
  6. concentrationconcentrated
  7. customto afford

출처 및 근거

ORD 기록
ord-1fcd7df2a64a4866982b62dddf2e34d4
출처 데이터셋
uspto-grants-2013_01
특허 번호
US08343968B2

연결된 노트

불러오는 중…