Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485056Generated: October 30, 2026

Bromomethyl 4-methoxyphenyl ketone → alpha(4-Picolylthio)-p-methoxyacetophenone

https://huagongshe.com/reaction/485056

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromomethyl 4-methoxyphenyl ketoneHCID 4965—
ReactantSodium MethoxideHCID 10942334—
ReactantPyridin-4-ylmethanethiolHCID 13092602—
SolventEthanolHCID 702—
Productalpha(4-Picolylthio)-p-methoxyacetophenoneHCID 1349031772.8%

Reaction Steps

Under a nitrogen atmosphere sodium methoxide (0.62 g., 11.4 mmoles) was dissolved in approximately 15 ml. of absolute ethanol and cooled in an ice bath. 4-Picolyl mercaptan (1.43 g., 11.4 mmoles) in approximately 3 ml. of absolute ethanol was added over approximately 5 minutes. After stirring for an additional 10 minutes, a slurry of alpha-bromo-p-methoxyacetophenone (2.62 g., 11.4 mmoles) in approximately 5 ml. of absolute ethanol was added over 10 minutes. The mixture was allowed to warm to room temperature and stirred for approximately 16 hours. The reaction mixture was concentrated to an oil containing solids, triturated with chloroform, salts removed by filtration and reconcentration to an oil (3.6 g.). The oil was chromatographed on 120 g. of silica gel with chloroform as eluant. Product containing fractions were combined and stripped to an oil which crystallized on trituration with cold ether. Filtration gave alpha(4-picolylthio)-p-methoxyacetophenone [2.27 g.; m.p. 64-65° C.; ir (KBr): 3-3.5, 5.95, 6.25, 7.95, 8.55, 12.0 and 12.2,μ mass spectra: m/e calcd: 273, found: 273, 150, 135, 124, 107, 92; pnmr/CDCl3 /TMS/delta: 6.35 (s, 2H), 6.3 (s, 2H), 6.1 (s, 3H), 3.1 (d, 2H), 2.7 (d, 2H), 2.0 (d, 2H), 1.4 (d, 2H)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04535084
Source datasetuspto-grants-1985_08
ORD IDord-98959c8ca08341dda887b646ae092eaf
Source noteuspto-grants-1985_08