2-Acetoxybenzoyl chloride → HCID 20516334, compound

HRID 1902337Notes

Reaction equation

HRID 1902337 reaction equation
[C:1]([O:4][C:5]1[CH:13]=[CH:12][CH:11]=[CH:10][C:6]=1[C:7](Cl)=[O:8])(=[O:3])[CH3:2].[NH2:14][C:15]1[C:26]([CH2:27][N:28]([CH2:31][CH3:32])[CH2:29][CH3:30])=[CH:25][C:18]([C:19]([O:21][CH2:22][CH2:23][OH:24])=[O:20])=[CH:17][C:16]=1[Br:33]>>[NH2:14][C:15]1[C:26]([CH2:27][N:28]([CH2:31][CH3:32])[CH2:29][CH3:30])=[CH:25][C:18]([C:19]([O:21][CH2:22][CH2:23][O:24][C:7](=[O:8])[C:6]2[CH:10]=[CH:11][CH:12]=[CH:13][C:5]=2[O:4][C:1](=[O:3])[CH3:2])=[O:20])=[CH:17][C:16]=1[Br:33]

Participants

3

Reactant 2

HCID 796682-Acetoxybenzoyl chlorideHCID 20516019HCID 20516019, compound

Product 1

HCID 20516334HCID 20516334, compound

Procedure

This compound was prepared from 2-acetoxybenzoyl chloride and 1-[4-amino-3-bromo-5-diethylaminomethyl-benzoyloxy]-2-hydroxy-ethane analogous to Example 5. Oil.

Sources & evidence

ORD record
ord-9610150981ca43609f926a525f5761ba
Source dataset
uspto-grants-1982_12
Patent number
US04362738

Reaction notes

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