Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42142Generated: October 27, 2026

Ammonium Chloride → 5-Bromo-2-(4-methanesulfonylbenzyloxy)pyridine

https://huagongshe.com/reaction/42142

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant2,5-DibromopyridineHCID 69353—
Reactant(4-Methanesulfonylphenyl)methanolHCID 3801026—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
Product5-Bromo-2-(4-methanesulfonylbenzyloxy)pyridineHCID 6708325631%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 2,5-dibromopyridine (474 mg, 2.00 mmol) and 4-(methanesulfonyl)benzyl alcohol (372 mg, 2.00 mmol) in tetrahydrofuran (5 mL) was cooled to −15° C. under N2 and potassium tert-butoxide (1.0M in tetrahydrofuran, 2.2 mL, 2.20 mmol) was added dropwise over 10 minutes. The mixture was stirred at 0° C. for 5.5 hours, poured into saturated aqueous ammonium chloride solution and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=1/1) to give the title compound (210 mg, yield 31%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536176B2
Source datasetuspto-grants-2013_09
ORD IDord-c78bc94182cb42c48b59f4800f97a3c8
Source noteuspto-grants-2013_09