Benzyl Bromide → HCID 21288490、化合物
反応式
[CH2:1](Br)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH:9][CH:10]([C:16]1[CH:17]=[C:18]([CH:20]=[CH:21][CH:22]=1)[NH2:19])[CH2:11][CH2:12][CH2:13][CH2:14][CH3:15]>>[OH:9][CH:10]([C:16]1[CH:17]=[C:18]([CH:20]=[CH:21][CH:22]=1)[NH:19][CH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)[CH2:11][CH2:12][CH2:13][CH2:14][CH3:15]参加物
3
実験手順
For compounds in which X is --NR2 --(CHR1)n --, the corresponding amino starting compounds are employed to form the desired amino compound. Thus, aniline is condensed with 3-(1-hydroxyhexyl)benzylbromide to form 2-[3-(1-hydroxyhexyl)benzylamino]benzene. Alternatively, benzyl bromide is condensed with 3-(1-hydroxyhexyl)aniline to form 2-[3-(1-hydroxyhexyl)anilinomethyl]benzene.
出典と根拠
- ORDレコード
- ord-92042b8a8b384e9c9c692acae5cb02c7
- 出典データセット
- uspto-grants-1988_10
- 特許番号
- US04778931
反応ノート
読み込み中…