m-Chloroperbenzoic acid → HCID 86745023、化合物

HRID 2249208ノート

反応式

HRID 2249208 の反応式
[C:1]([OH:4])(=[O:3])[CH3:2].[C:5]([OH:8])(=[O:7])[CH3:6].[CH3:9][O:10][C:11]1[CH:17]=[C:16]([OH:18])[C:15]([CH2:19][CH:20]=[C:21]([CH3:23])[CH3:22])=[CH:14][C:12]=1[OH:13].ClC1C=CC=C(C(OO)=[O:32])C=1>ClCCl>[C:1]([OH:4])(=[O:3])[CH3:2].[C:5]([OH:8])(=[O:7])[CH3:6].[O:32]1[C:21]([CH3:23])([CH3:22])[CH:20]1[CH2:19][C:15]1[C:16]([OH:18])=[CH:17][C:11]([O:10][CH3:9])=[C:12]([CH:14]=1)[OH:13]

参加物

4

反応条件

温度
5 °C

実験手順

To a solution of 2-methoxy-5-(3-methyl-2-butenyl)hydroquinone diacetate (2.84 g) in dichloromethane (40 ml) was added m-chloroperbenzoic acid (2.09 g, 80% purity) in several portions at 5° C. After the addition, the mixture was stirred for one hour at 5° C., washed twice with a mixture of aqueous sodium bicarbonate solution and aqueous sodium thiosulfinate solution, dried, and concentrated in vacuo. The residue was crystallized from n-hexane to give 5-(2,3-epoxy-3-methylbutyl)-2-methoxyhydroquinone diacetate as a white solid (2.93 g).

後処理

  1. additionAfter the addition
  2. washwashed twice with a mixture of aqueous sodium bicarbonate solution and aqueous sodium thiosulfinate solution
  3. customdried
  4. concentrationconcentrated in vacuo
  5. customThe residue was crystallized from n-hexane

出典と根拠

ORDレコード
ord-bd65eb4a9f974a7d8fef2368e1b47585
出典データセット
uspto-grants-1991_08
特許番号
US05043354

反応ノート

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