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2-Benzyl-5,6-dimethoxyisoindoline → 5,6-Dimethoxyisoindoline

HRID 704457
ノート
印刷プレビュー

反応式

HRID 704457 の反応式
C([N:8]1[CH2:16][C:15]2[C:10](=[CH:11][C:12]([O:19][CH3:20])=[C:13]([O:17][CH3:18])[CH:14]=2)[CH2:9]1)C1C=CC=CC=1>CO.[C].[Pd]>[CH3:18][O:17][C:13]1[CH:14]=[C:15]2[C:10](=[CH:11][C:12]=1[O:19][CH3:20])[CH2:9][NH:8][CH2:16]2
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

HCID 149937372-Benzyl-5,6-dimethoxyisoindoline

生成物 1

HCID 200743515,6-Dimethoxyisoindoline収率 77.3%

試薬・触媒・溶媒 2

HCID 178418390HCID 178418390、化合物触媒HCID 887Methanol溶媒

実験手順

1.20 g (4.46 mmol) of 2-benzyl-5,6-dimethoxyisoindoline was dissolved in 40 ml of methanol at 40° C., and 84 mg of 10% palladium carbon was added thereto. Under a hydrogen stream, catalytic reduction was conducted at the same temperature for 4 hours. The solvent was distilled off under reduced pressure, and a small amount of ethyl acetate and diethylether was added to the residue and stirred. The precipitates were collected to obtain 617 mg (yield: 77.3%) of the above identified compound.

後処理

  1. distillationThe solvent was distilled off under reduced pressure
  2. additiona small amount of ethyl acetate and diethylether was added to the residue
  3. customThe precipitates were collected
  4. customto obtain 617 mg (yield: 77.3%) of the

出典と根拠

ORDレコード
ord-ad7730c17b25490ab447e050783a9c6c
出典データセット
uspto-grants-1991_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04987235

反応ノート

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