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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716402Generated: October 30, 2026

4-Bromophenacyl bromide → HCID 86689666, compound

https://huagongshe.com/reaction/716402

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromophenacyl bromideHCID 7454—
Reactant4-(Heptyloxy)benzothioamideHCID 12680596—
SolventIsopropanolHCID 3776—
ProductHCID 86689666HCID 8668966641.6%

Reaction Steps

To a stirring mixture of 4-(heptyloxy)benzothioamide (1.30 g, 5.17 mmol) in isopropanol (20 mL) was added 2-bromo-1-(4-bromophenyl)ethanone (1.44 g, 5.17 mmol). The precipitate was collected by filtration and washed with EtOH (2×5 mL). The filter cake was slurried with NaHCO3 (2×20 mL), water (2×20 mL) then EtOH (2×5 mL) and dried to afford 926 mg (41%) of 4-(4-bromophenyl)-2-(4-(heptyloxy)phenyl)thiazole as a pale yellow powder. LCMS-ESI (m/z) calculated for C22H24BrNOS: 429.1. found 430.0 [M+H]+, tR=3.41 min. (Method 4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187522B2
Source datasetuspto-grants-2015_11
ORD IDord-3b5e78daeb094b5ca5e801409321756f
Source noteuspto-grants-2015_11