3-Boc-2,2-dimethyloxazolidine-4-carboxaldehyde, (S)-(-)- → HCID 10946477, 화합물

HRID 238572

반응식

HRID 238572 반응식
[C:1]([O:5][C:6]([N:8]1[C@H:12]([CH:13]=[O:14])[CH2:11][O:10][C:9]1([CH3:16])[CH3:15])=[O:7])([CH3:4])([CH3:3])[CH3:2].[F:17][C:18]([Si](C)(C)C)([F:20])[F:19].[F-].C([N+](CCCC)(CCCC)CCCC)CCC>C1COCC1.[F-].C([N+](CCCC)(CCCC)CCCC)CCC>[CH3:15][C:9]1([CH3:16])[N:8]([C:6]([O:5][C:1]([CH3:4])([CH3:3])[CH3:2])=[O:7])[C@H:12]([CH:13]([OH:14])[C:18]([F:20])([F:19])[F:17])[CH2:11][O:10]1

참가 물질

6

실험 절차

To a mixture of (S)-4-formyl-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester (1.0 g, 4.36 mmol), (trifluoromethyl)trimethylsilane (2.0 M solution in THF, 2.6 mL, 5.20 mmol) in THF (10 mL) was added tetrabutylammonium fluoride (1.0 M solution in THF, 0.1 mL, 0.10 mmol) at 0° C. After addition, the mixture was stirred at room temperature for 60 h. Then, tetrabutylammonium fluoride (1.0 M solution in THF, 9 mL, 9.0 mmol) was added and the mixture stirred for another 6 h and subsequently quenched by adding saturated aq. NaHCO3 solution, extracted with EtOAc. The extracts were washed with saturated aq. NaHCO3 solution, water, brine and dried over Na2SO4. Concentration and purification gave (S)-tert-butyl 2,2-dimethyl-4-(2,2,2-trifluoro-1-hydroxyethyl)oxazolidine-3-carboxylate (1.21 g, 92%), which showed a complicated NMR spectrum because of the different comformers.

후처리

  1. additionAfter addition
  2. stirringthe mixture stirred for another 6 h
  3. customsubsequently quenched
  4. additionby adding saturated aq. NaHCO3 solution
  5. extractionextracted with EtOAc
  6. washThe extracts were washed with saturated aq. NaHCO3 solution, water, brine
  7. dry with materialdried over Na2SO4
  8. concentrationConcentration and purification

출처 및 근거

ORD 기록
ord-93324d6f5b2344c5b14a673db5d4e78e
출처 데이터셋
uspto-grants-2014_02
특허 번호
US08642632B2

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