ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

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

HRID 1369594
ノート
印刷プレビュー

反応式

HRID 1369594 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 addition 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. additionThe aqueous layer was made acidic by addition of conc sulfuric acid
  6. extractionThe acidic water solution was extracted with diethyl ether
  7. washthe organic layer was washed with water
  8. dry with materialdried (Na2SO4)
  9. customevaporated under reduced pressure

出典と根拠

ORDレコード
ord-412d421ae5e04513b37b3166611d2af2
出典データセット
uspto-grants-2003_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06579884B1

反応ノート

読み込み中…

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