Phosphorus tribromide → (6-Bromohex-3-en-1-yl)benzene
反応式
[C:1]1([CH2:7][CH2:8][CH:9]([CH:11]2[CH2:13][CH2:12]2)O)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.P(Br)(Br)[Br:15].[Br-].[Li+]>[Br-].[Zn+2].[Br-]>[C:1]1([CH2:7][CH2:8][CH:9]=[CH:11][CH2:12][CH2:13][Br:15])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1参加物
5
実験手順
[V; Ar is C6H5, R is H] was prepared from 16.5 g. of 2-phenylethyl cyclopropyl carbinol (Preparation B6), 21.5 g. of phosphorus tribromide, 17.65 g. of lithium bromide and 20.7 g. of zinc bromide according to the procedure given above in Preparation C1, affording 21 g. of product as a pale yellow oil.
後処理
- custom[V; Ar is C6H5, R is H] was prepared from 16.5 g
- customaffording 21 g
出典と根拠
- ORDレコード
- ord-a8548b045b8b49bf81e5a2911e66dda9
- 出典データセット
- uspto-grants-1978_06
- 特許番号
- US04093736
反応ノート
読み込み中…