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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501268Generated: October 25, 2026

Bromine → Phenacyl bromide

https://huagongshe.com/reaction/501268

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant4'-PhenoxyacetophenoneHCID 236783—
ProductPhenacyl bromideHCID 6259—

Reaction Steps

4-Phenoxyacetophenone was brominated with bromine according to Method A to provide the desired α-bromoacetophenone, which was condensed with 2-amino-1,3,4,-thiadiazole-5-sulfonamide according to method C, to provide compound 87 as an off white solid. 1H NMR (200 MHz, DMSO-d6) δ 8.82 (s, 1H), 8.71 (s, 2H), 7.90 (d, J=7.9 Hz, 2H), 7.40 (t, J=7.3 Hz, 2H), 7.07 (t, J=7.3 Hz, 1H), 7.08-7.03 (m, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772260B2
Source datasetuspto-grants-2010_08
ORD IDord-8bfbfe3959c148d9bed9f6cb3ab2818e
Source noteuspto-grants-2010_08