6-Aminohexanoic Acid → 6-Aminohexanoic Acid

HRID 979744Notes

Reaction equation

HRID 979744 reaction equation
[C:1]([Cl:11])(=[O:10])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH3:9].[NH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][C:18]([OH:20])=[O:19]>>[C:1]([Cl:11])(=[O:10])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH3:9].[NH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][C:18]([OH:20])=[O:19].[C:1]([NH:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][C:18]([OH:20])=[O:19])(=[O:10])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH3:9]

Participants

5

Reactant 2

HCID 5646-Aminohexanoic AcidHCID 69819Nonanoyl chloride

Product 3

HCID 5646-Aminohexanoic AcidHCID 69819Nonanoyl chlorideHCID 11022006Hexanoic acid, 6-[(1-oxononyl)amino]-

Procedure

N-nonanoyl-6-aminocaproic acid was prepared by reaction of nonanoyl chloride with 6-aminocaproic acid according to the procedure described in Example I. From 67.3 g (0.381 mol) of nonanoyl chloride and 50.0 g (0.381 mol) of 6-aminocaproic acid was obtained 103 g of N-nonanoyl-6-aminocaproic acid, mp 71°-74° C.

Sources & evidence

ORD record
ord-f8bde2f8c91d4b4c9ed5db484bf39870
Source dataset
uspto-grants-1987_01
Patent number
US04634551

Reaction notes

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