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Methanethiol → Ethyl 2-ethylthiomethyl-4-methylpentanoate

HRID 374700
ノート
印刷プレビュー

反応式

HRID 374700 の反応式
[CH2:1]([C:5](=[CH2:11])[C:6]([O:8][CH2:9][CH3:10])=[O:7])[CH:2]([CH3:4])[CH3:3].C[C:13]([CH3:16])([O-])C.[K+].C[SH:19]>C(OCC)(=O)C>[CH2:13]([S:19][CH2:11][CH:5]([CH2:1][CH:2]([CH3:4])[CH3:3])[C:6]([O:8][CH2:9][CH3:10])=[O:7])[CH3:16]
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 878MethanethiolHCID 10909818Ethyl 4-methyl-2-methylenepentanoateHCID 23665647Potassium tert-butoxide

生成物 1

HCID 22418875Ethyl 2-ethylthiomethyl-4-methylpentanoate

試薬・触媒・溶媒 1

HCID 8857Ethyl Acetate溶媒

実験手順

650 mg of ethyl 2-isobutyl-2-propenoate was dissolved in 3 ml of methylmercaptan, and 50 mg of potassium tert-butoxide was added thereto. The mixture was stirred at room temperature for two hours. The reaction solution was diluted with 60 ml of ethyl acetate, washed with water and then with a saturated sodium chloride aqueous solution and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure to obtain 660 mg of ethyl 2-ethylthiomethyl-4-methylpentanoate as colorless oily substance.

後処理

  1. washwashed with water
  2. dry with materialwith a saturated sodium chloride aqueous solution and dried over anhydrous sodium sulfate
  3. distillationThe solvent was distilled off under reduced pressure

出典と根拠

ORDレコード
ord-0611cdcfcdfa4a28afd654b3317d8f93
出典データセット
uspto-grants-1996_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05481036

反応ノート

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