Dimethyl Sulfide → (E,E)-Farnesyl chloride

HRID 248569

反応式

HRID 248569 の反応式
[Cl:1]N1C(=O)CCC1=O.CSC.O[CH2:13]/[CH:14]=[C:15](/[CH2:17][CH2:18]/[CH:19]=[C:20](/[CH2:22][CH2:23][CH:24]=[C:25]([CH3:27])[CH3:26])\[CH3:21])\[CH3:16]>ClCCl>[CH2:13]([Cl:1])/[CH:14]=[C:15](/[CH2:17][CH2:18]/[CH:19]=[C:20](/[CH2:22][CH2:23][CH:24]=[C:25]([CH3:27])[CH3:26])\[CH3:21])\[CH3:16]

参加物

5

実験手順

A solution of N-chlorosuccinimide (6.8 g, 50.9 mmol) in dry dichloromethane (338 ml) was cooled to -30 ° and dimethylsulfide (4.1 ml, 55.3 mmol) was added dropwise over 3 min. After 13 min., the cooling bath was removed and the mixture was stirred for 30 min. The mixture was cooled to -40 ° and a solution of (E,E)-farnesol (11.3 ml, 44 mmol) in 112 ml dichloromethane was added over 10 min. The cooling bath was removed and the mixture was stirred for 30 min. The temperature of the reaction mixture rose to 0° and a clear solution was obtained. After stirring for two more hours the solvent (about 400 ml) was removed on a rotary evaporator and the material was taken up in hexane (600 ml). The solution was washed with ice cold water (3×90 ml) and cold brine (2×35 ml) and then dried (MgSO4). The solvent was removed under vacuum at ambient temperature and finally dried under pump vacuum to give 11.0 g (100%) of title compound as a pale yellow liquid.

後処理

  1. customthe cooling bath was removed
  2. temperatureThe mixture was cooled to -40 °
  3. customThe cooling bath was removed
  4. stirringthe mixture was stirred for 30 min
  5. customrose to 0°
  6. customa clear solution was obtained
  7. customwas removed on a rotary evaporator
  8. washThe solution was washed with ice cold water (3×90 ml) and cold brine (2×35 ml)
  9. dry with materialdried (MgSO4)
  10. customThe solvent was removed under vacuum at ambient temperature
  11. customfinally dried under pump vacuum

出典と根拠

ORDレコード
ord-8f93fe0f46cf417b8a9ef94846fa3e48
出典データセット
uspto-grants-1993_05
特許番号
US05210262

関連ノート

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