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

HRID 459540
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인쇄 미리보기

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HRID 459540 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]>>[C:34]([O:38][C:15]([NH:12][CH:1]1[CH2:6][CH2:5][CH:4]=[CH:3][CH2:2]1)=[O:24])([CH3:37])([CH3:36])[CH3:35]
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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 (dichloromethane) and then repurified by column chromatography on silica gel (hexane:ethyl acetate=20:1) to obtain the title compound (24.9 g) as colorless crystals.

후처리

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

출처 및 근거

ORD 기록
ord-3b45d73126e84f98b495975b9943f3b2
출처 데이터셋
uspto-grants-2007_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07192968B2

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