2-Mercaptoethanol → 3-(2-Chloroethyl)-5,6-dihydro-1,4-oxathiin

HRID 620804

反応式

HRID 620804 の反応式
Cl[CH:2]([CH2:6][CH2:7][Cl:8])[C:3](=[O:5])C.[SH:9][CH2:10][CH2:11]O.C(N(CC)CC)C>C1(C)C=CC=CC=1>[Cl:8][CH2:7][CH2:6][C:2]1[S:9][CH2:10][CH2:11][O:5][CH:3]=1

参加物

5

実験手順

A mixture of the 3,5-dichloro-2-pentanone (39 g., 0.24 mole) and 2-mercaptoethanol (20 g., 0.26 mole) in toluene (250 ml) was stirred, and triethylamine (27 g., 0.27 mole) added dropwise thereto. After stirring overnight at ambient temperature, the mixture was washed with dilute hydrochloric acid and subsequently refluxed with p-toluenesulfonic acid (0.5 g.) with azeotropic removal of water for 4 hours. Upon cooling, the reaction mixture was washed with aqueous sodium bicarbonate, dried (magnesium sulfate), and the toluene removed to leave the product 3-(2-chloroethyl)-5,6-dihydro-1,4-oxathiin (bp. 62°-70°/0.025 mm) in 60% yield and 98% purity (G.C.). N.M.R. spectrum (Deuterchloroform) gave lambda values: 1.85 (3H,S) 2.3-2.65 (2H,t); 2.9-3.5 (2H,t); 3.95-3.7 (2H,t); 4.1-4.25 (2H,t).

後処理

  1. stirringAfter stirring overnight at ambient temperature
  2. washthe mixture was washed with dilute hydrochloric acid
  3. temperaturesubsequently refluxed with p-toluenesulfonic acid (0.5 g.) with azeotropic removal of water for 4 hours
  4. temperatureUpon cooling
  5. washthe reaction mixture was washed with aqueous sodium bicarbonate
  6. dry with materialdried (magnesium sulfate)
  7. customthe toluene removed

出典と根拠

ORDレコード
ord-3b55fa7e3dfd495abd4277ce47da7530
出典データセット
uspto-grants-1989_04
特許番号
US04822813

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