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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1525286Generated: November 4, 2026

3-Bromobenzaldehyde → HCID 89462449, compound

https://huagongshe.com/reaction/1525286

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromobenzaldehydeHCID 76583—
ReactantBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
Reactanttert-Butylsulfinamide, (S)-(-)-HCID 11355477—
CatalystCopper SulfateHCID 24462—
SolventDichloromethaneHCID 6344—
ProductHCID 89462449HCID 8946244952%

Reaction Conditions

Temperature37 °C

Reaction Steps

3-bromobenzaldehyde, 24-a, (30 g, 162 mmol) in dichloromethane (600 ml) were added (S)-2-methylpropane-2-sulfinamide (23.52 g, 194.5 mmol), PPTS (5.97 g, 16.2 mmol) and anhydrous CuSO4 (78 g, 486 mmol) and the resulting mixture was stirred at 37° C. overnight. The mixture was then filtrated and the filtrate was concentrated under vacuum. The residue was purified by column chromatography (petroleum ether/ethyl acetate=5/1) to provide the product, 25-a, (24.5 g, 52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079930B2
Source datasetuspto-grants-2015_07
ORD IDord-9b4311da15b54bca82d590c9d5616fee
Source noteuspto-grants-2015_07