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

HRID 431301
ノート
印刷プレビュー

反応式

HRID 431301 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 were suspended in 10 ml of ethanol and placed in an ultrasonic bath for 4 h. The reaction mixture was then acidified with 2N HCl and stirred. The ethanol was distilled off, water and dichloromethane were added to the residue and the mixture was extracted with dichloromethane. The organic phase was separated off, dried over MgSO4, filtered and concentrated and the residue was purified chromatographically on silica gel using dichloromethane/methanol 20/1. This gave 5-chloro-2-methylsulfonylindan-1-ol of melting point 163° C.

後処理

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

出典と根拠

ORDレコード
ord-1f8ec30a2c7f42bc9b66f70f68cca59f
出典データセット
uspto-grants-2003_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06657086B2

反応ノート

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