Acetic Acid → N-(4-bromo-2-methoxy-6-nitrophenyl)acetamide

HRID 44475

反応式

HRID 44475 の反応式
[Br:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[C:5]([NH2:11])=[C:4]([O:12][CH3:13])[CH:3]=1.OS(O)(=O)=O.[CH3:19][C:20](O)=[O:21]>CC(OC(C)=O)=O>[Br:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[C:5]([NH:11][C:20](=[O:21])[CH3:19])=[C:4]([O:12][CH3:13])[CH:3]=1

参加物

5

反応物 3

HCID 176Acetic AcidHCID 1118Sulfuric AcidHCID 508790564-Bromo-2-methoxy-6-nitroaniline

生成物 1

HCID 53491145N-(4-bromo-2-methoxy-6-nitrophenyl)acetamide収率 75%

試薬・触媒・溶媒 1

HCID 7918Acetic Anhydride溶媒

反応条件

温度
70 °C

実験手順

To a solution of 4-bromo-2-methoxy-6-nitrobenzenamine (27.85 g) in HOAc (150 mL) and Ac2O (17 mL) was added conc. H2SO4 at 70° C. and the mixture was stirred at 70° C. for 30 min and kept at rt overnight. The formed precipitate was collected by filtration and washed with hexane to afford the desired product as a light yellow solid (24.45 g, 75%). 1H NMR (300 MHz, DMSO-d6) δ ppm 2.01 (s, 3H), 3.92 (s, 3H), 7.61 (d, 1H, J=1.8 Hz), 7.65 (d, 1H, J=1.8 Hz), 9.91 (s, 1H); LC-MS: m/e=289 [M+1]+

後処理

  1. waitkept at rt overnight
  2. filtrationThe formed precipitate was collected by filtration
  3. washwashed with hexane

出典と根拠

ORDレコード
ord-05be219954e84e998756ab0b54497e7c
出典データセット
uspto-grants-2013_09
特許番号
US08541411B2

関連ノート

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