Sodium Hydroxide → HCID 21521247, compound

HRID 918584Notes

Reaction equation

C([S:9][CH:10]([CH3:22])[C:11]([NH:13][CH:14]([CH3:21])[CH2:15][CH2:16][CH2:17][C:18]([OH:20])=[O:19])=[O:12])(=O)C1C=CC=CC=1.[OH-].[Na+]>>[SH:9][CH:10]([CH3:22])[C:11]([NH:13][CH:14]([CH3:21])[CH2:15][CH2:16][CH2:17][C:18]([OH:20])=[O:19])=[O:12]

Participants

Reactant 2

HCID 14798Sodium Hydroxide

HCID 53649967HCID 53649967, compound

Product 1

HCID 21521247HCID 21521247, compoundYield 61.8%

Procedure

12.4g of N-(2-benzoylmercaptopropionyl)-5-aminocaproic acid was hydrolized with NaOH in a similar manner as described in Example VIII to give 5.2g of N-(2-mercaptopropionyl)-5-aminocaproic acid, ##EQU12##

Sources & evidence

ORD record: ord-00de7fac010e417c85a23efcdd4f0cb0
Source dataset: uspto-grants-1976_07
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US03971828

Reaction notes

Loading…