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Lithium Hydroxide → 3-Chloro-4-(4-methyl-2-oxo-oxazolidin-3-yl)-benzoic acid

HRID 2094319
ノート
印刷プレビュー

反応式

HRID 2094319 の反応式
[Cl:1][C:2]1[CH:3]=[C:4]([CH:10]=[CH:11][C:12]=1[N:13]1[CH:17]([CH3:18])[CH2:16][O:15][C:14]1=[O:19])[C:5]([O:7]CC)=[O:6].[OH-].[Li+]>CO>[Cl:1][C:2]1[CH:3]=[C:4]([CH:10]=[CH:11][C:12]=1[N:13]1[CH:17]([CH3:18])[CH2:16][O:15][C:14]1=[O:19])[C:5]([OH:7])=[O:6]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 3939Lithium HydroxideHCID 67048447Ethyl 3-chloro-4-(4-methyl-2-oxo-oxazolidin-3-yl)-benzoate

生成物 1

HCID 667314913-Chloro-4-(4-methyl-2-oxo-oxazolidin-3-yl)-benzoic acid

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

0.90 g (3.17 mmol) ethyl 3-chloro-4-(4-methyl-2-oxo-oxazolidin-3-yl)-benzoate are stirred for 1 hour in 50 ml of methanol with 10 ml 1-molar aqueous lithium hydroxide solution at ambient temperature. The mixture is then evaporated down to 20 ml i. vac., acidified with conc. hydrochloric acid and extracted with ethyl acetate. The combined organic phases are washed with sat. sodium chloride solution, dried over sodium sulphate and evaporated down i. vac. The residue is crystallised from a little diethyl ether and suction filtered.

後処理

  1. customThe mixture is then evaporated down to 20 ml i
  2. extractionextracted with ethyl acetate
  3. washThe combined organic phases are washed with sat. sodium chloride solution
  4. dry with materialdried over sodium sulphate
  5. customevaporated down i
  6. customThe residue is crystallised from a little diethyl ether and suction
  7. filtrationfiltered

出典と根拠

ORDレコード
ord-7d3b973fd6a041da8dbd4b95592da6e9
出典データセット
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08445525B2

反応ノート

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