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Hydrazine hydrate (1:1) → (2S)-2-(4-Fluorophenyl)propan-1-amine

HRID 2276739
ノート
印刷プレビュー

反応式

HRID 2276739 の反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C@H:8]([CH3:21])[CH2:9][N:10]2C(=O)C3C(=CC=CC=3)C2=O)=[CH:4][CH:3]=1.O.NN>C1(C)C=CC=CC=1>[F:1][C:2]1[CH:3]=[CH:4][C:5]([C@H:8]([CH3:21])[CH2:9][NH2:10])=[CH:6][CH:7]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 24654Hydrazine hydrate (1:1)HCID 67453498(S)-2-(2-(4-Fluorophenyl)propyl)isoindoline-1,3-dione

生成物 1

HCID 28267524(2S)-2-(4-Fluorophenyl)propan-1-amine収率 100.2%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

反応条件

温度
80 °C

実験手順

To a room-temperature solution of (S)-2-(2-(4-fluorophenyl)propyl)isoindoline-1,3-dione (900 mg, 3.2 mmol, 1.0 equiv) in toluene (14 mL) was added hydrazine hydrate (1.4 mL, 45 mmol, 14 equiv) by syringe. The resulting mixture was heated to 80° C. for 30 minutes and then cooled to room temperature. The resulting solution was decanted from the solid in the reaction mixture, and the solid was washed with additional toluene. The combined organic layers were combined and concentrated in vacuo to provide the title compound (491 mg, 99%), which was used without further purification.

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート

後処理

  1. temperaturecooled to room temperature
  2. customThe resulting solution was decanted from the solid in the reaction mixture
  3. washthe solid was washed with additional toluene
  4. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-623998cec767480fbf85f2f631c5d2e7
出典データセット
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09133123B2

反応ノート

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