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Hydrochloric Acid → 5-Chloro-2-methylsulfonylindan-1-ol

HRID 433326
ノート
印刷プレビュー

反応式

HRID 433326 の反応式
[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[C:7](=[O:11])[CH:6]([S:12]([CH3:15])(=[O:14])=[O:13])[CH2:5]2.[BH4-].[Na+].Cl>C(O)C>[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[CH:7]([OH:11])[CH:6]([S:12]([CH3:15])(=[O:14])=[O:13])[CH2:5]2
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 313Hydrochloric AcidHCID 4311764Sodium borohydrideHCID 99648205-Chloro-2-methylsulfonylindan-1-one

生成物 1

HCID 98347545-Chloro-2-methylsulfonylindan-1-ol

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

0.489 g (2 mmol) of 5-chloro-2-methylsulfonylindan-1-one and 0.095 g (2.5 mmol) of sodium borohydride are suspended in 10 ml of ethanol and placed in an ultrasonic bath for 4 h. The reaction mixture is then acidified with 2N HCl and stirred. The ethanol is distilled off, water and dichloromethane are added to the residue and the mixture is extracted with dichloromethane. The organic phase is separated off, dried over MgSO4, filtered and concentrated and the residue is purified chromatographically on silica gel using dichloromethane/methanol 20/1. This gives 5-chloro-2-methylsulfonylindan-1-ol of melting point 163° C.

後処理

  1. distillationThe ethanol is distilled off
  2. additionwater and dichloromethane are added to the residue
  3. extractionthe mixture is extracted with dichloromethane
  4. customThe organic phase is separated off
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customthe residue is purified chromatographically on silica gel

出典と根拠

ORDレコード
ord-314cccc883d54964b8a42ceec1782929
出典データセット
uspto-grants-2003_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06667345B2

反応ノート

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