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tert-Butanol → tert-Butyl cyclohex-3-en-1-ylcarbamate

HRID 902849
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인쇄 미리보기

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HRID 902849 반응식
[CH:1]1(C(O)=O)[CH2:6][CH2:5][CH:4]=[CH:3][CH2:2]1.C([N:12]([CH2:15]C)CC)C.C1(P(N=[N+]=[N-])(C2C=CC=CC=2)=[O:24])C=CC=CC=1.[C:34]([OH:38])([CH3:37])([CH3:36])[CH3:35]>>[CH:1]1([NH:12][C:15](=[O:24])[O:38][C:34]([CH3:37])([CH3:36])[CH3:35])[CH2:6][CH2:5][CH:4]=[CH:3][CH2:2]1
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참가 물질

5

반응물 4

HCID 6386tert-ButanolHCID 8471TriethylamineHCID 209033-Cyclohexene-1-carboxylic acidHCID 199401P,P-Diphenylphosphinic azide

생성물 1

HCID 11063381tert-Butyl cyclohex-3-en-1-ylcarbamate

반응 조건

온도
90 °C

실험 절차

3-Cyclohexene-1-carboxylic acid (25.3 g) was dissolved in tert-butanol (250 ml), triethylamine (28 ml) and diphenylphosphorylazide (43.0 ml) were added, and the mixture was stirred for 1 hour at room temperature and 2 days at 90° C. The solvent was distilled off under reduced pressure, and the residue was purified by column chromatography on silica gel (methylene chloride) and then repurified by column chromatography on silica gel (hexane:ethyl acetate=20:1) to obtain the title compound (24.9 g).

후처리

  1. distillationThe solvent was distilled off under reduced pressure
  2. customthe residue was purified by column chromatography on silica gel (methylene chloride)
  3. customrepurified by column chromatography on silica gel (hexane:ethyl acetate=20:1)

출처 및 근거

ORD 기록
ord-e94fb2062ed34f5197512518284b633e
출처 데이터셋
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07365205B2

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