2-(4-Chlorophenyl)-3-methylbutanoyl chloride → (4-Chlorophenyl)isopropylketene

HRID 2119057

反応式

HRID 2119057 の反応式
[CH:1]([CH:4]([C:8]1[CH:13]=[CH:12][C:11]([Cl:14])=[CH:10][CH:9]=1)[C:5](Cl)=[O:6])([CH3:3])[CH3:2]>C(Cl)Cl.C(N(CC)CC)C.CCCCCCC>[Cl:14][C:11]1[CH:10]=[CH:9][C:8]([C:4]([CH:1]([CH3:3])[CH3:2])=[C:5]=[O:6])=[CH:13][CH:12]=1

参加物

5

実験手順

To a solution of 2.31 g of isopropyl(4-chlorophenyl)acetyl chloride in 10 ml of methylene chloride was added in one portion 1.5 g of triethylamine. After 18 hours, 15 ml of heptane was added to the mixture and the triethylamine hydrochloride was removed by filtration. The filtrate was stripped and 10 ml of heptane was added and the resulting mixture was filtered and stripped to give a yellow residue, which was dissolved in 5 ml heptane for GLC analysis. The resulting solution was distilled through a Bantam-ware short-neck head from an oil bath at 125°-150° C. and head temperature of 110°-100° C. at 0.2-0.05 mm to give 0.95 g of distillate and 0.81 g of gum. The distillate was crystallized twice from 2 volumes of hexane at -80° C. The solid was melted and stripped to about 40° C. at 0.5 mm to give 0.42 g of the desired product as a yellow liquid.

後処理

  1. customthe triethylamine hydrochloride was removed by filtration
  2. addition10 ml of heptane was added
  3. filtrationthe resulting mixture was filtered
  4. customto give a yellow residue, which
  5. distillationThe resulting solution was distilled through a Bantam-ware short-neck head from an oil bath at 125°-150° C.

出典と根拠

ORDレコード
ord-10d117f4500d40a1b24f832f34662622
出典データセット
uspto-grants-1987_07
特許番号
US04681947

関連ノート

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