Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349720Generated: October 30, 2026

2-Chloroacetophenone → HCID 12664904, compound

https://huagongshe.com/reaction/349720

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloroacetophenoneHCID 10757—
ReactantPotassium ethanethioateHCID 23670855—
SolventAcetoneHCID 180—
ProductHCID 12664904HCID 12664904—

Reaction Steps

2-Chloroacetophenone in acetone (3.10 g, 200 ml) was added potassium thioacetate (2.80 g, 1.2 equivalents) and the reaction mixture was stirred overnight at RT. The salt precipitate was filtered off and the filtrate was concentrated. The residue was purified by flash chromatography on silica gel to give 2.04 g of α-thioacetyl acetophenone as orange reddish oil. 1H NMR (500 MHz, CHLOROFORM-D) δ ppm 7.98–8.02 (2 H, m) 7.60 (1 H, t, J=7.48 Hz) 7.48 (2 H, t, J=7.78 Hz) 4.40 (2 H, s) 2.41 (3 H, s). MS [ESI, MNa+] m/z calcd for C10H10O2SNa 217.04, found 217.16.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179926B2
Source datasetuspto-grants-2007_02
ORD IDord-206fed69242048efa66e90f5e5608284
Source noteuspto-grants-2007_02