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Water → 2-(2-Bromo-3-methylphenyl)acetic acid

HRID 1006698
ノート
印刷プレビュー

反応式

HRID 1006698 の反応式
[Br:1][C:2]1[C:10]([CH3:11])=[CH:9][CH:8]=[CH:7][C:3]=1[CH2:4][C:5]#N.S(=O)(=O)(O)[OH:13].[OH2:17]>C(OCC)C>[Br:1][C:2]1[C:10]([CH3:11])=[CH:9][CH:8]=[CH:7][C:3]=1[CH2:4][C:5]([OH:13])=[O:17]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 962Water2 回HCID 1118Sulfuric AcidHCID 226726132-(2-Bromo-3-methylphenyl)acetonitrile

生成物 1

HCID 183574462-(2-Bromo-3-methylphenyl)acetic acid

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

実験手順

2-bromo-3-methylbenzylcyanid (8.8 g, 42 mmol) was added to a mixture of conc sulfuric acid (50 ml) and water (60 ml) and was refluxed overnight. Water (150 ml) and diethyl ether were added and the organic layer was separated. To the organic layer was added a saturated sodium bicarbonate solution and the aqueous layer was separated. The aqueous layer was made acidic by additon of conc sulfuric acid. The acidic water solution was extracted with diethyl ether and the organic layer was washed with water, dried (Na2SO4) and evaporated under reduced pressure to give 6.5 g of the title compound.

後処理

  1. temperaturewas refluxed overnight
  2. customthe organic layer was separated
  3. additionTo the organic layer was added a saturated sodium bicarbonate solution
  4. customthe aqueous layer was separated
  5. extractionThe acidic water solution was extracted with diethyl ether
  6. washthe organic layer was washed with water
  7. dry with materialdried (Na2SO4)
  8. customevaporated under reduced pressure

出典と根拠

ORDレコード
ord-a531a3da22ea44cdbed049cffe203659
出典データセット
uspto-grants-2004_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06790960B2

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート