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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873337Generated: October 27, 2026

Pyridine → 2-[6-(2-Bromo-acetoxy)-naphthalen-2-yl]-propionic acid methyl ester

https://huagongshe.com/reaction/1873337

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBromoacetyl chlorideHCID 89602—
Reactant2-(6-Hydroxy-naphthalen-2-yl)-propionic acid methyl esterHCID 598897—
SolventDichloromethaneHCID 6344—
Product2-[6-(2-Bromo-acetoxy)-naphthalen-2-yl]-propionic acid methyl esterHCID 5808371345.9%

Reaction Steps

To a solution of 2-(6-hydroxy-naphthalen-2-yl)-propionic acid methyl ester (20 grams) and pyridine (10.3 grams) in dichloromethane (200 ml) maintained at 0-5° C. under N2 atmosphere was added dropwise bromoacetyl chloride (19.6 grams). The reaction was stirred at the same temperature for one hour. The reaction mixture was washed with water (500 ml) and 5% solution of sodium carbonate followed by drying over sodium sulphate and distillation to get crude compound, which was purified by column chromatography using hexane as eluant to get pure 2-[6-(2-bromo-acetoxy)-naphthalen-2-yl]-propionic acid methyl ester (14 grams) as a dark brown syrup. The pure product was characterized using 1H NMR spectroscopy in CDCl3 δ 1.55 (d, 3H, CH3), 3.65 (s, 3H, Ester), 3.82 (q, 1H, CH), 4.08 (s, 2H, OCH2) 7.20 (dd, 1H, Ar), 7.4 (dd, 1H, Ar), 7.57 (d, 1H, Ar), 7.72 (d, 1H, Ar), 7.78 (d, 1H, Ar), 7.84 (d, 1H, Ar).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08303978B2
Source datasetuspto-grants-2012_11
ORD IDord-b3a6352071c1492f8d60f1fcf93a3c65
Source noteuspto-grants-2012_11