Acetyl chloride → Methyl 4-[4-(chloroacetyl)phenoxy]butyrate
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
- 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
読み込み中…