p-(2-Chlorophenyl)cinnamic acid → beta-(2'-Chloro-4-biphenylyl)propionic acid

HRID 1659065

反応式

HRID 1659065 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[CH:18]=[CH:17][C:11]([CH:12]=[CH:13][C:14]([OH:16])=[O:15])=[CH:10][CH:9]=1.[H][H]>[Pt]=O.C(O)C>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[CH:18]=[CH:17][C:11]([CH2:12][CH2:13][C:14]([OH:16])=[O:15])=[CH:10][CH:9]=1

参加物

5

反応物 2

HCID 54534814p-(2-Chlorophenyl)cinnamic acidHCID 178418361HCID 178418361、化合物

生成物 1

HCID 1394276beta-(2'-Chloro-4-biphenylyl)propionic acid

試薬・触媒・溶媒 2

HCID 82844Platinum oxide (PtO)触媒HCID 702Ethanol溶媒

実験手順

A suspension of 100 g of p-(2-chlorophenyl)cinnamic acid in 1 l. of 95% ethanol is hydrogenated at atmospheric pressure using platinum oxide catalyst (1 g). The uptake of hydrogen ceases when approximately 9-10 l. of hydrogen is consumed. The catalyst is then filtered off and the reaction evaporated to dryness to give β-(2'-chloro-4-biphenylyl)propionic acid.

後処理

  1. customof hydrogen is consumed
  2. filtrationThe catalyst is then filtered off
  3. customthe reaction evaporated to dryness

出典と根拠

ORDレコード
ord-828198b8ce5a45dc8b17d5737e10150b
出典データセット
uspto-grants-1976_06
特許番号
US03966801

関連ノート

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