Acetyl chloride → Methyl 4-[4-(chloroacetyl)phenoxy]butyrate

HRID 2419371ノート

反応式

HRID 2419371 の反応式
[O:1]([CH2:8][CH2:9][CH2:10][C:11]([O:13][CH3:14])=[O:12])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(Cl)(=O)C.[Cl:19][CH2:20][C:21](C1C=CC(CCC(O)=O)=CC=1)=[O:22]>>[Cl:19][CH2:20][C:21]([C:5]1[CH:6]=[CH:7][C:2]([O:1][CH2:8][CH2:9][CH2:10][C:11]([O:13][CH3:14])=[O:12])=[CH:3][CH:4]=1)=[O:22]

参加物

4

実験手順

Methyl 4-phenoxybutyrate was reacted with acetyl chloride in a similar manner to that described above for 3-[4-(chloroacetyl)phenyl]propionic acid, except that the crude product was triturated with petrol to give methyl 4-[4-(chloroacetyl)phenoxy]butyrate as a crystalline solid which was pure by TLC analysis (on silica plates; eluant: 50% ether/50% petrol).

後処理

  1. customwas triturated with petrol

出典と根拠

ORDレコード
ord-9689b62e9f2347318eed30e79ef37ac8
出典データセット
uspto-grants-1978_08
特許番号
US04105790

反応ノート

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