Acetone → 1,2,10-Decanetriol

HRID 248108

반응식

HRID 248108 반응식
[CH2:1]([OH:11])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7]CC=C.[CH3:12][C:13]([CH3:15])=[O:14].C[N+]([O-:20])(C)C.S(=O)(O)[O-].[Na+]>C(O)(C)(C)C.[Os](=O)(=O)(=O)=O.O>[CH2:12]([OH:20])[CH:13]([OH:14])[CH2:15][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][CH2:1][OH:11]

참가 물질

8

반응물 4

HCID 180AcetoneHCID 1145Trimethylamine oxideHCID 256129-Decen-1-olHCID 23665763Sodium Bisulfite

생성물 1

HCID 27359121,2,10-Decanetriol

시약·촉매·용매 3

HCID 30318Osmium Tetroxide촉매HCID 962Water용매HCID 6386tert-Butanol용매2회

실험 절차

9-Decen-1-ol (25.0 g, 160 mmol) was dissolved in a solution made up of t-butanol (100 ml), acetone (90 ml) and water (10 ml). To this solution was added trimethylamine-N-oxide (26.6 g, 240 mmol) and 2 ml of a solution of osmium tetroxide (50 mg) in t-butanol (25 ml). The resulting solution was stirred 20 hours under nitrogen then 10% sodium bisulfite was added (50 ml). The mixture was concentrated then taken up in trichloromethane and washed 2 times with water, dried with Na2SO4 and concentrated to give 1,2,10-decanetriol as an oil. This material was used without further purification in preparation of the corresponding acetonide (of formula 21).

후처리

  1. concentrationThe mixture was concentrated
  2. washwashed 2 times with water
  3. dry with materialdried with Na2SO4
  4. concentrationconcentrated

출처 및 근거

ORD 기록
ord-2c8d5436cfde4a7188a8eb296c6719a9
출처 데이터셋
uspto-grants-1993_05
특허 번호
US05208036

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