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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485057Generated: October 30, 2026

2-Bromo-4'-nitroacetophenone → alpha-(4-Picolylthio)p-nitroacetophenone

https://huagongshe.com/reaction/485057

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-4'-nitroacetophenoneHCID 66840—
ReactantSodium MethoxideHCID 10942334—
ReactantPyridin-4-ylmethanethiolHCID 13092602—
SolventEthanolHCID 702—
Productalpha-(4-Picolylthio)p-nitroacetophenoneHCID 20271287—

Reaction Steps

Under a nitrogen atmosphere, sodium methoxide (0.52 g., 9.6 mmoles) was dissolved in 15 ml. of absolute ethanol and cooled to 0°-5° C. 4-Picolyl mercaptan (1.2 g., 9.6 mmoles) in 15 ml. of ethanol was added over 5 minutes time. Alpha-bromo-p-nitro-acetophenone (2.3 g., 9.6 mmoles) in 20 ml. of warm ethanol was then added over 5 minutes, the mixture was warmed to room temperature and left to stir for approximately 16 hours. The reaction mixture was filtered and the filtrate concentrated to an oil (4.3 g.). The oil was chromatographed on 175 g. of silica gel with 1:1 hexane:ethyl acetate as eluant. Product-containing fractions were combined and evaporated to yield alpha-(4-picolylthio)-p-nitro-acetophenone [1.40 g.; oil; pnmr/CDCl3 /TMS/delta: 6.5 (3, 4H), 2.7 (d, 2H), 1.9 (d, 4H), 1.5 (d, 2H); mass spectra: m/e calcd.: 288; found: 288, 242, 165, 150, 138, 124, 104, 92, 76, 65, 39; ir (film): 3-3.5, 5.95, 6.25, 6.55, 7.35, 7.85, 11.70,μ].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04535084
Source datasetuspto-grants-1985_08
ORD IDord-6f0d5520f9814793b8c87a202d5766af
Source noteuspto-grants-1985_08