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Methanol → 4-({[4-(Methylsulfanyl)phenyl]sulfanyl}-methyl)bicyclo[4.1.0]heptane-3-carboxylic acid

HRID 2222908
ノート
印刷プレビュー

反応式

HRID 2222908 の反応式
[CH3:1][S:2][C:3]1[CH:8]=[CH:7][C:6]([S:9][CH2:10][CH:11]2[CH2:17][CH:16]3[CH:14]([CH2:15]3)[CH2:13][CH:12]2[C:18]([O-:20])=[O:19])=[CH:5][CH:4]=1.CO.[OH-].[Li+]>COCCOC>[CH3:1][S:2][C:3]1[CH:8]=[CH:7][C:6]([S:9][CH2:10][CH:11]2[CH2:17][CH:16]3[CH:14]([CH2:15]3)[CH2:13][CH:12]2[C:18]([OH:20])=[O:19])=[CH:5][CH:4]=1
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 887MethanolHCID 3939Lithium HydroxideHCID 865961304-({[4-(Methylsulfanyl)phenyl]-sulfanyl}-methyl)bicyclo[4.1.0]heptane-3-carboxylate

生成物 1

HCID 865961294-({[4-(Methylsulfanyl)phenyl]sulfanyl}-methyl)bicyclo[4.1.0]heptane-3-carboxylic acid

試薬・触媒・溶媒 1

HCID 80711,2-Dimethoxyethane溶媒

実験手順

Methyl(1S/R,3R/S,4R/S,6R/S)-4-({[4-(methylsulfanyl)phenyl]-sulfanyl}-methyl)bicyclo[4.1.0]heptane-3-carboxylate was dissolved in ethylene glycol dimethyl ether (3.0 mL) and methanol (1 mL) in a 25 mL round bottom flask. Aqueous solution of lithium hydroxide (3.0 mL, 6.0 mmol, 2 M) was added and the reaction mixture was stirred at ambient temperature for 36 h. After acidification with 2 M aqueous hydrochloric acid to pH 3, the product was extracted into ether. The combined ether extracts were washed with saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, and concentrated by rotary evaporation to give (1S/R,3R/S,4R/S,6R/S)-4-({[4-(methylsulfanyl)phenyl]sulfanyl}-methyl)bicyclo[4.1.0]heptane-3-carboxylic acid.

後処理

  1. extractionAfter acidification with 2 M aqueous hydrochloric acid to pH 3, the product was extracted into ether
  2. washThe combined ether extracts were washed with saturated aqueous sodium chloride solution
  3. dry with materialdried over anhydrous sodium sulfate
  4. concentrationconcentrated by rotary evaporation

出典と根拠

ORDレコード
ord-261755d5415a43999f19965235f7850d
出典データセット
uspto-grants-2008_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07371747B2

反応ノート

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