Sulfuric Acid → Methyl 3-bromo-5-nitrobenzoate

HRID 1243362

反応式

HRID 1243362 の反応式
[N+:1]([C:4]1[CH:5]=[C:6]([CH:11]=[CH:12][CH:13]=1)[C:7]([O:9][CH3:10])=[O:8])([O-:3])=[O:2].S(=O)(=O)(O)O.[Br:19]Br>S(=O)(=O)(O)O.S([O-])([O-])(=O)=O.[Ag+2].CO>[Br:19][C:12]1[CH:11]=[C:6]([CH:5]=[C:4]([N+:1]([O-:3])=[O:2])[CH:13]=1)[C:7]([O:9][CH3:10])=[O:8]

参加物

7

反応物 3

HCID 1118Sulfuric AcidHCID 24408BromineHCID 69260Methyl 3-nitrobenzoate

生成物 1

HCID 239341Methyl 3-bromo-5-nitrobenzoate収率 72%

試薬・触媒・溶媒 3

HCID 1118Sulfuric Acid触媒HCID 178418844HCID 178418844、化合物触媒HCID 887Methanol溶媒

反応条件

温度
90 °C

実験手順

A mixture of methyl 3-nitrobenzoate (122 g, 674 mmol), silver sulphate (100 g, 320.7 mmol) and concentrated sulfuric acid (750 mL) was stirred mechanically and heated at 90° C. To this mixture was added bromine (37 mL), dropwise, over 2 h. The reaction was stirred another hour, cooled and filtered. The filtrate was mixed with 2 L water and 1 Kg crushed ice. The solid was filtered and dried to afford a mixture of the desired methyl ester and free acid hydrolysis product. The mixture was taken up into methanol (1 L), treated with 10 drops concentrated sulfuric acid and refluxed for 12 h. The reaction mixture was allowed to cool and the crystals that were deposited were collected and dried in a desiccator to afford 126 g (72% yield) of methyl 3-bromo-5-nitrobenzoate (EX-119A): 1H NMR (300 MHz, CDCl3) δ 8.65 (s, 1H), 8.44 (s, 1H), 8.37 (s, 1H), 3.94 (s, 3H).

後処理

  1. stirringThe reaction was stirred another hour
  2. temperaturecooled
  3. filtrationfiltered
  4. additionThe filtrate was mixed with 2 L water and 1 Kg
  5. customcrushed ice
  6. filtrationThe solid was filtered
  7. customdried
  8. customto afford
  9. temperaturerefluxed for 12 h
  10. temperatureto cool
  11. customthe crystals that were deposited were collected
  12. customdried in a desiccator

出典と根拠

ORDレコード
ord-19b2dd6100e14109b7c4f2fb640df9d7
出典データセット
uspto-grants-2006_10
特許番号
US07119094B1

関連ノート

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