4-Bromobenzaldehyde → HCID 9866579, compound

HRID 278153Notes

Reaction equation

[Br:1][C:2]1[CH:15]=[CH:14][C:5]([CH2:6][S:7]([CH2:10][C:11](O)=O)(=[O:9])=[O:8])=[CH:4][CH:3]=1.[Br:16][C:17]1[CH:24]=[CH:23][C:20](C=O)=[CH:19][CH:18]=1>>[Br:1][C:2]1[CH:15]=[CH:14][C:5]([CH2:6][S:7](/[CH:10]=[CH:11]/[C:20]2[CH:23]=[CH:24][C:17]([Br:16])=[CH:18][CH:19]=2)(=[O:9])=[O:8])=[CH:4][CH:3]=1

Participants

Reactant 2

HCID 707414-Bromobenzaldehyde

HCID 22065316[(4-Bromophenyl)methanesulfonyl]acetic acid

Product 1

HCID 9866579HCID 9866579, compoundYield 88%

Procedure

A solution of 4-bromobenzyl sulfonylacetic acid (0.01 mol) and 4-bromobenzaldehyde (0.01 mol) was subjected to Procedure 1. The title compound was obtained in 88% yield.

Sources & evidence

ORD record: ord-6c15aa1a06f44f54b2a578c989959204
Source dataset: uspto-grants-2002_03
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06359013B1

Reaction notes

Loading…