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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1794034Generated: November 2, 2026

Phenacyl bromide → HCID 22220812, compound

https://huagongshe.com/reaction/1794034

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
ReactantAcetonitrileHCID 6342—
Reactant1-(1,3-Thiazol-2-yl)ethan-1-olHCID 9989295—
SolventWaterHCID 962—
ProductHCID 22220812HCID 2222081242.9%

Reaction Steps

1-(2-Thiazolyl)ethanol (0.71 g, 5.49 mmole), 2-bromo-1-phenyl-1-ethanone (1.09 g, 5.47 mmole), and acetonitrile (0.6 mL) were combined and heated with stirring at 130 C for 4 hr. After cooling, water (20 mL) was added and the mixture was filtered and extracted twice with ether. The aqueous layer was treated with active carbon and filtered to give a clear solution which was concentrated in vacuo to 1.52 g of residue, which was crystallized from acetonitrile/ether and recrystallized twice from methanol/acetonitrile/ether to give 0.77 g of the title compound as prisms, mp 157–158 C; calc'd for C13H)4NO2SBr: C, 47.55; H, 4.33; N, 4.26; found: C, 47.52; H, 4.32; N, 4.14.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022721B1
Source datasetuspto-grants-2006_04
ORD IDord-2789532dd2474eec844fbd02e14a2727
Source noteuspto-grants-2006_04