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

HRID 2194557
ノート
印刷プレビュー

反応式

HRID 2194557 の反応式
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
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

HCID 124113305-Bromo-3-methyl-1,2-benzoxazole収率 65.1%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

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.

後処理

  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)

出典と根拠

ORDレコード
ord-4e8c991aaa9f47048766b590973032ac
出典データセット
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08334292B1

反応ノート

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