Benzyl Bromide → 3-Benzyloxy-4-hydroxymethylbenzonitrile
反応式
[CH:1]([C:3]1[CH:10]=[CH:9][C:6]([C:7]#[N:8])=[CH:5][C:4]=1[OH:11])=[O:2].[CH2:12](Br)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.C([O-])([O-])=O.[K+].[K+].[BH4-].[Na+]>CO.C1COCC1>[CH2:12]([O:11][C:4]1[CH:5]=[C:6]([CH:9]=[CH:10][C:3]=1[CH2:1][OH:2])[C:7]#[N:8])[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1参加物
6
実験手順
33.1 g of 4-formyl-3-hydroxybenzonitrile (Liebigs Ann. Chem. (1982) 1836) were O-benzylated with 1 eq. each of benzyl bromide and K2CO3 and, after workup, reduced with NaBH4 in 100 ml of MeOH/THF 2:3 at −10° C. to 0° C. to give the alcohol. 22.4 g were obtained. The product could be crystallized from DCM/petroleum ether.
出典と根拠
- ORDレコード
- ord-302acd40a98e4854af95f15444e1bce4
- 出典データセット
- uspto-grants-2005_05
- 特許番号
- US06900319B2
反応ノート
読み込み中…