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2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 5-Bromo-3-methyl-1,2-benzoxazole

HRID 2194557
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HRID 2194557 반응식
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.ClC1C(=O)C(C#N)=C(C#N)C(=O)C=1Cl.[Br:34][C:35]1[CH:36]=[CH:37][C:38]([OH:45])=[C:39](/[C:41](=[N:43]/O)/[CH3:42])[CH:40]=1>C(Cl)Cl>[Br:34][C:35]1[CH:36]=[CH:37][C:38]2[O:45][N:43]=[C:41]([CH3:42])[C:39]=2[CH:40]=1
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참가 물질

5

반응물 3

HCID 67752,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 11776TriphenylphosphineHCID 1355380141-(5-Bromo-2-hydroxyphenyl)ethanone oxime

생성물 1

HCID 124113305-Bromo-3-methyl-1,2-benzoxazole수율 65.1%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a stirred solution of triphenylphosphine (6.8 g, 26.1 mmol) and 2,3-dichloro-5,6-dicyanobenzoquinone (DDQ) (3.9 g, 26.1 mmol) in CH2Cl2 (50 mL) was added (E)-1-(5-bromo-2-hydroxyphenyl)ethanone oxime (11) (5.0 g, 21.73 mmol) in small portions over a period of 15 min. The mixture was stirred for additional 10 min at room temperature and then the solvent was removed under reduced pressure. The residue was purified by flash column chromatography (silica gel, eluting with 5% ethyl acetate and hexanes) to give the title compound (12) (3.0 g, 65%) as a brown solid. 1H NMR (CDCl3, 400 MHz) δ 7.79 (s, 1H), 7.40 (dd, J=8.4, 1.6 Hz, 1H), 7.35 (d, J=8.4 Hz, 1H), 2.64 (s, 3H); MS (ESI, M+H+) C8H7BrNO, calcd. 212.0. found 212.0, 214.0.

후처리

  1. customthe solvent was removed under reduced pressure
  2. customThe residue was purified by flash column chromatography (silica gel, eluting with 5% ethyl acetate and hexanes)

출처 및 근거

ORD 기록
ord-4e8c991aaa9f47048766b590973032ac
출처 데이터셋
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08334292B1

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