tert-Butanol → tert-butyl N-(5-bromo-2-chlorophenyl)carbamate

HRID 1803604

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HRID 1803604 반응식
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([Cl:11])=[C:6]([CH:10]=1)C(O)=O.C1(P(N=[N+]=[N-])(C2C=CC=CC=2)=[O:19])C=CC=CC=1.CC[N:31]([CH2:34]C)CC.[C:36]([OH:40])([CH3:39])([CH3:38])[CH3:37]>>[C:36]([O:40][C:34](=[O:19])[NH:31][C:6]1[CH:10]=[C:2]([Br:1])[CH:3]=[CH:4][C:5]=1[Cl:11])([CH3:39])([CH3:38])[CH3:37]

참가 물질

5

실험 절차

A solution of 5-Bromo-2-Chloro benzoic acid (24 g, 0.1 mol), di-phenylphosphoryl azide (28 mL, 1.3 eq), and Et3N (140 mL, 10 eq) in tert-butanol (300 mL) was refluxed for 3 hrs. The resulting solution was concentrated under reduced pressure, diluted with ether (300 mL) and washed with HCl 1N (300 mL), saturated solution of NaHCO3 (200 mL), and brine (200 mL). The organic layers was dried over anhydrous sodium sulfate and concentrated. Chromatography on silica (EtOAc/n-hexane) yielded, (26 g, 85%).

후처리

  1. concentrationThe resulting solution was concentrated under reduced pressure
  2. additiondiluted with ether (300 mL)
  3. washwashed with HCl 1N (300 mL), saturated solution of NaHCO3 (200 mL), and brine (200 mL)
  4. dry with materialThe organic layers was dried over anhydrous sodium sulfate
  5. concentrationconcentrated
  6. customChromatography on silica (EtOAc/n-hexane) yielded

출처 및 근거

ORD 기록
ord-c568271e01884979a91252abcd2887f4
출처 데이터셋
uspto-grants-2013_01
특허 번호
US08349836B2

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