Trichloroacetyl chloride → HCID 13924057、化合物

HRID 569223ノート

反応式

HRID 569223 の反応式
[Cl:1][C:2]([Cl:7])(Cl)[C:3](Cl)=[O:4].P(Cl)(Cl)(Cl)=O.[CH2:13]([O:15][CH:16]([CH2:26][CH3:27])[CH2:17][CH2:18][CH2:19][CH2:20][CH:21]1[CH2:25][CH2:24][CH:23]=[CH:22]1)[CH3:14].C(=O)(O)[O-].[Na+]>CCOCC.[Zn].[Cu]>[Cl:1][C:2]1([Cl:7])[CH:24]2[CH:25]([CH:21]([CH2:20][CH2:19][CH2:18][CH2:17][CH:16]([O:15][CH2:13][CH3:14])[CH2:26][CH3:27])[CH2:22][CH2:23]2)[C:3]1=[O:4]

参加物

7

実験手順

A solution containing trichloroacetyl chloride (187 g, 1.03 moles) and phosphorous oxychloride (158 g, 1.03 moles), both dissolved in 500 ml ether (1700 ml) is added dropwise to a reaction vessel containing zinc/copper couple (75 g, 1.15 moles), 3-(5-ethoxyheptyl)cyclopentene (170 g, 0.573 moles), and ether (1700 ml). After the addition is complete the reaction is refluxed for 4 hours. The reaction vessel is cooled to room temperature and the mixture neutralized by adding it to a saturated solution of sodium bicarbonate. The solution is filtered, the phases separated, and the aqueous layer is extracted with ether. The organic phases are combined and dried over anhydrous sodium sulfate. The solvent is removed under vacuum leaving a clear yellow oil. The crude product is fractionally distilled under vacuum leaving the product as a clear, colorless oil of 7,7-dichloro-4-(5-ethoxyheptyl)bicyclo [3.2.0]heptan 6-one, BP 145° C./0.3 mm.

後処理

  1. additionis added dropwise to a reaction vessel
  2. additionAfter the addition
  3. temperatureis refluxed for 4 hours
  4. filtrationThe solution is filtered
  5. customthe phases separated
  6. extractionthe aqueous layer is extracted with ether
  7. dry with materialdried over anhydrous sodium sulfate
  8. customThe solvent is removed under vacuum
  9. customleaving a clear yellow oil
  10. distillationThe crude product is fractionally distilled under vacuum

出典と根拠

ORDレコード
ord-da5f1477e5fc4e5984fd3e6494f2e109
出典データセット
uspto-grants-1988_03
特許番号
US04731458

反応ノート

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