Sodium Cyanide → HCID 14500538, compound
Reaction equation
Br[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][NH:9][C:10]1[CH:15]=[CH:14][C:13]([OH:16])=[CH:12][CH:11]=1.[C-:17]#[N:18].[Na+]>CS(C)=O>[OH:16][C:13]1[CH:14]=[CH:15][C:10]([NH:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][C:17]#[N:18])=[CH:11][CH:12]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
8-[(4-Hydroxyphenyl)amino]octanenitrile was prepared in 80% yield from 33.2 g [0.11 mol] of 4-[(7-bromoheptyl)amino]phenol and 26.5 g (0.52 mol) of sodium cyanide by the first procedure of Example 2, part d, except that DMSO was used in place of DMF as the solvent.
Sources & evidence
- ORD record
- ord-b44418e135bf428682c735d533d515dc
- Source dataset
- uspto-grants-1989_05
- Patent number
- US04835180
Reaction notes
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