Chlorotrimethylsilane → HCID 18403070, 화합물

HRID 377171노트

반응식

HRID 377171 반응식
[CH2:1]([PH:5](=[O:7])[OH:6])[CH2:2][CH2:3][CH3:4].C(N(CC)CC)C.C[Si](Cl)(C)C.[CH2:20]([O:27][C:28]([CH:30]([CH2:43][CH2:44][C:45]([O:47][CH2:48][C:49]1[CH:54]=[CH:53][CH:52]=[CH:51][CH:50]=1)=[O:46])[CH2:31]P(C)(=O)OCC1C=CC=CC=1)=[O:29])[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1>ClCCl>[CH2:1]([P:5]([CH2:31][CH:30]([C:28]([O:27][CH2:20][C:21]1[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=1)=[O:29])[CH2:43][CH2:44][C:45]([O:47][CH2:48][C:49]1[CH:50]=[CH:51][CH:52]=[CH:53][CH:54]=1)=[O:46])(=[O:6])[OH:7])[CH2:2][CH2:3][CH3:4]

참가 물질

6

반응물 4

HCID 6397ChlorotrimethylsilaneHCID 8471TriethylamineHCID 158852182,4-Di(benzyloxycarbonyl)butyl(methyl)-O-benzylphosphinic acidHCID 178454911HCID 178454911, 화합물

생성물 1

HCID 18403070HCID 18403070, 화합물수율 40.6%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

반응 조건

온도
0 °C

실험 절차

Butylphosphinic acid (2.0 g, 16mmol) in 80 mL of dry dichloromethane was cooled to 0C under an atmosphere of nitrogen. Triethylamine (6.7 g, 66 mmol) was added followed by trimethylsilyl chloride (58 mL, 58 mmol, 1.0 M in dichloromethane). The mixture was stirred at 0° C. for 10 minutes and dibenzyl 2-methylenepentanedioate (2)(6.4 g, 20 mmol) in 20 mL of dichloromethane was added. The cold bath was removed and the reaction warmed to room temperature and stirred overnight. The mixture was then cooled to 0° C. and quenched by the slow addition of 5% hydrochloric acid. The dichloromethane layer was then removed and washed with 5% hydrochloric acid and with brine. The organic layer was dried (MgSO4) and evaporated to give a clear light golden liquid. The liquid was purified by flash chromatography and eluted with 3:1 hexane/ethyl acetate containing 5% acetic acid. The desired fractions were combined and evaporated to give butyl[2,4-di(benzyloxycarbonyl)butyl]phosphinic acid (3,R=n-butyl, R1=H) (2.9 g, 40w) as a clear and colorless oil. Rf 0.12 (3:1, Hex./EtOAc 5% AcOH).

후처리

  1. customThe cold bath was removed
  2. temperaturethe reaction warmed to room temperature
  3. stirringstirred overnight
  4. temperatureThe mixture was then cooled to 0° C.
  5. customquenched by the slow addition of 5% hydrochloric acid
  6. customThe dichloromethane layer was then removed
  7. washwashed with 5% hydrochloric acid and with brine
  8. dry with materialThe organic layer was dried (MgSO4)
  9. customevaporated
  10. customto give a clear light golden liquid
  11. customThe liquid was purified by flash chromatography
  12. washeluted with 3:1 hexane/ethyl acetate containing 5% acetic acid
  13. customevaporated

출처 및 근거

ORD 기록
ord-c3f087a97dea40938050d65c2fc13926
출처 데이터셋
uspto-grants-2000_02
특허 번호
US06025344

반응 노트

불러오는 중…