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Hydrochloric Acid → 4-Chloro-3-ethylthio-2-methylbenzoic acid

HRID 1640387
ノート
印刷プレビュー

反応式

HRID 1640387 の反応式
C(=O)([O-])[O-].[Cs+].[Cs+].[Cl:7][C:8]1[CH:16]=[CH:15][C:11]([C:12]([OH:14])=[O:13])=[C:10]([CH3:17])[C:9]=1[SH:18].I[CH2:20][CH3:21].Cl>C(#N)C.O>[Cl:7][C:8]1[CH:16]=[CH:15][C:11]([C:12]([OH:14])=[O:13])=[C:10]([CH3:17])[C:9]=1[S:18][CH2:20][CH3:21]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 313Hydrochloric AcidHCID 6340IodoethaneHCID 10796Cesium carbonateHCID 667391434-Chloro-3-mercapto-2-methylbenzoic acid

生成物 1

HCID 667391774-Chloro-3-ethylthio-2-methylbenzoic acid収率 92%

試薬・触媒・溶媒 2

HCID 962Water溶媒
HCID 6342
Acetonitrile
溶媒

実験手順

3.71 g (11.3 mmol) of cesium carbonate were added to 1.10 g (5.42 mmol) of 4-chloro-3-mercapto-2-methylbenzoic acid in 20 ml of acetonitrile. The reaction mixture was stirred at RT for 10 min, and 1.02 g (6.51 mmol) of iodoethane were then slowly added dropwise. The reaction mixture was then stirred at RT for 16 h. The solvent was then removed, and a mixture of 20 ml of methanol and 2 ml of 20% strength aqueous sodium hydroxide solution was then added to the reaction mixture. For the hydrolysis of the ethyl ester formed, the mixture was stirred at RT for 16 h and then freed from the solvents. The residue was taken up in water and acidified with diluted HCl, and the mixture was stirred at RT for 10 min and then filtered. The residue was washed with water and sucked dry. 1.15 g of clean product were isolated.

後処理

  1. stirringThe reaction mixture was then stirred at RT for 16 h
  2. customThe solvent was then removed
  3. additiona mixture of 20 ml of methanol and 2 ml of 20% strength aqueous sodium hydroxide solution
  4. additionwas then added to the reaction mixture
  5. customFor the hydrolysis of the ethyl ester
  6. customformed
  7. stirringthe mixture was stirred at RT for 16 h
  8. stirringthe mixture was stirred at RT for 10 min
  9. filtrationfiltered
  10. washThe residue was washed with water
  11. customsucked dry

出典と根拠

ORDレコード
ord-febf48003a774154aad8ad5c33643acd
出典データセット
uspto-grants-2012_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08114816B2

反応ノート

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