5-Chloro-2-methoxybenzoyl chloride → HCID 20304389, compound

HRID 1732659Notes

Reaction equation

HRID 1732659 reaction equation
Cl.[NH2:2][CH2:3][C:4]1[CH:9]=[CH:8][C:7]([CH2:10][CH2:11][C:12]([O:14]CC)=[O:13])=[CH:6][CH:5]=1.[Cl:17][C:18]1[CH:19]=[CH:20][C:21]([O:27][CH3:28])=[C:22]([CH:26]=1)[C:23](Cl)=[O:24]>>[Cl:17][C:18]1[CH:19]=[CH:20][C:21]([O:27][CH3:28])=[C:22]([CH:26]=1)[C:23]([NH:2][CH2:3][C:4]1[CH:5]=[CH:6][C:7]([CH2:10][CH2:11][C:12]([OH:14])=[O:13])=[CH:8][CH:9]=1)=[O:24]

Participants

3

Reactant 2

HCID 123841765-Chloro-2-methoxybenzoyl chlorideHCID 20304428Ethyl 3-[4-(aminomethyl)phenyl]propanoate--hydrogen chloride (1/1)

Product 1

HCID 20304389HCID 20304389, compound

Procedure

By reaction of ethyl β-[4-(aminomethyl)-phenyl]-propionate hydrochloride (m.p. 192°-193° C.) with 5-chloro-2-methoxybenzoyl chloride, there is obtained β-[4-(5-chloro-2-methoxybenzamidomethyl)-phenyl]-propionic acid; m.p. 152°-153° C., after recrystallization from isopropanol.

Sources & evidence

ORD record
ord-5b3809bb76ab462f8df9762737cf5c53
Source dataset
uspto-grants-1980_12
Patent number
US04238506

Reaction notes

Loading…