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

HRID 922697
ノート
印刷プレビュー

反応式

HRID 922697 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.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 9321HydrazineHCID 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 (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 concentrated in vacuo to provide the title compound (491 mg, 99%), which was used without further purification. m/z=154.2 [M+H]+.

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. concentrationThe combined organic layers were concentrated in vacuo

出典と根拠

ORDレコード
ord-c830a77e07d041a5b1b419899799c294
出典データセット
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09278962B2

反応ノート

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