2-Bromo-3-fluoro-6-nitroaniline → 3-Bromo-4-fluorobenzene-1,2-diamine

HRID 1056098ノート

反応式

HRID 1056098 の反応式
[Br:1][C:2]1[C:8]([F:9])=[CH:7][CH:6]=[C:5]([N+:10]([O-])=O)[C:3]=1[NH2:4]>[Pt].CCO>[Br:1][C:2]1[C:8]([F:9])=[CH:7][CH:6]=[C:5]([NH2:10])[C:3]=1[NH2:4]

参加物

4

反応物 1

HCID 194297802-Bromo-3-fluoro-6-nitroaniline

生成物 1

HCID 533953903-Bromo-4-fluorobenzene-1,2-diamine

試薬・触媒・溶媒 2

HCID 23939Platinum触媒HCID 702Ethanol溶媒

実験手順

A 500 mL round-bottomed flask containing Pt/C (5%, 6.00 g, 1.54 mmol) and 2-bromo-3-fluoro-6-nitroaniline (600b) (20.85 g, 89 mmol) were treated with EtOH (250 mL) and stirred under an atmosphere of H2 (balloon) for 22 h. LC-MS indicated ca. 35% conversion to the desired material (M+1=204.9/206.9). Another balloon of H2 was added and it was stirred for another 16 h resulting in >90% conversion to the desired product (M+1=204.9/207.1) by LC-MS. The suspension was filtered through a plug of Celite washing with EtOH and concentrated affording crude 3-bromo-4-fluorobenzene-1,2-diamine (18 g, 88 mmol, 99% yield) as a black/purple viscous oil. 1H NMR (400 MHz, CDCl3) δ ppm 6.60 (1H, dd, J=8.5, 5.2 Hz), 6.42-6.50 (1H, m). 19F NMR (376 MHz, CDCl3) δ ppm −116.48 (1F, s). m/z (ESI, +ve ion) 204.9/206.9 (M+H)+.

後処理

  1. additionAnother balloon of H2 was added
  2. stirringit was stirred for another 16 h

出典と根拠

ORDレコード
ord-f5fe1325420149b1a47b1827ab20498c
出典データセット
uspto-grants-2016_07
特許番号
US09394297B2

反応ノート

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