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Methanethiol → Ethyl 2-ethylthiomethyl-4-methylpentanoate

HRID 1109404
ノート
印刷プレビュー

反応式

HRID 1109404 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-3ebab7d9a46b42388645c404b5ea24c2
出典データセット
uspto-grants-1994_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05319082

反応ノート

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