Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1796418Generated: November 3, 2026

Bromomethyl 4-methoxyphenyl ketone → HCID 12330847, compound

https://huagongshe.com/reaction/1796418

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromomethyl 4-methoxyphenyl ketoneHCID 4965—
ReactantPotassium ethanethioateHCID 23670855—
SolventEthanolHCID 702—
ProductHCID 12330847HCID 1233084781.6%

Reaction Steps

Potassium thioacetate (2.28 g, 20 mmol) was added to a solution of 2-bromo-4′-methoxy acetophenone (4.58 g, 20 mmol) in absolute ethanol (150 ml). The reaction was stirred at ambient temperature under nitrogen for 16 hours at which time the white precipitate that had formed was filtered and the ethanol removed at reduced pressure. The residue was dissolved in dichloromethane (250 ml) and washed with water (200 ml), brine (200 ml), dried over Na2SO4 and the solvent removed at reduced pressure. The resulting residue was chromatographed on silica with a gradient from 10%-35% ethyl acetate in hexane to yield 3.4 g (76%) of 2-thioacetyl-4′-methoxy acetophenone. 1H NMR (CDCl3) δ2.36 p (s, 3h), 3.84 (s, 3h), 4.33 (s, 2h), 6.9 (d, 2h, J=9.2 Hz), 7.9 (d, 2h, J=9.2 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07030153B2
Source datasetuspto-grants-2006_04
ORD IDord-bbff1082066c4a14b504fe9b49789d53
Source noteuspto-grants-2006_04