반응 #49100

ord-9c53447d44cc4e7e8f74a8e8f8979bc9

반응 방정식

CN(C)C1(C#N)CCCC1
D1
CN(C)C1(C#N)CCCC1
1-(dimethylamino)cyclopentanecarbonitrile
[Li][c]1ccccc1
phenyl lithium
[BH4-].[Na+]
sodium borohydride
CN(C)C1(C(N)c2ccccc2)CCCC1
D2
CN(C)C1(C(N)c2ccccc2)CCCC1
Racemic {1-[amino(phenyl)methyl]cyclopentyl}dimethylamine
CN(C)C1(C#N)CCCCC1
1-(dimethylamino)cyclohexanecarbonitrile
CNC.Cl
dimethylamine hydrochloride
O=C1CCCCC1
cyclohexanone
[C-]#N.[K+]
potassium cyanide
CN(C)C1(C(N)c2ccccc2)CCCCC1
title compound
수율 36.0%
CN(C)C1(C(N)c2ccccc2)CCCCC1
(±){1-[Amino(phenyl)methyl]cyclohexyl}dimethylamine
수율 36.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

실험 절차

The title compound was prepared in two stages from (i) dimethylamine hydrochloride (3.26 g, 0.04 mol), cyclohexanone (3.9 g, 0.04 mol) and potassium cyanide (2.60 g, 0.04 mol) in water (25 ml) in a similar manner to that described in D1 to make 1-(dimethylamino)cyclohexanecarbonitrile (6.6 g, 100%). This was reacted directly in (ii) with phenyl lithium in dibutyl ether (10.5 ml of a 1.9M solution, 0.02 mol) in THF (30 ml) followed by sodium borohydride (1.51 g, 0.04 mol) in a similar manner to that described in D2 to afford the title compound (2.5 g, 36%). 1H NMR (CDCl3) δ: 0.85 (1H, m), 1.00 (1H, m), 1.25 (2H, m), 1.35-1.60 (6H, br m), 1.70 (1H, m), 2.10 (1H, m), 2.46 (6H, s), 4.15 (1H, s), 7.20-7.32 (5H, m).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07745642B2uspto-grants-2010_06