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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1059660Generated: October 31, 2026

Oxalyl chloride → 6-bromo-3-benzyloxy-4-methoxypyridine-2-carbonyl Chloride

https://huagongshe.com/reaction/1059660

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 22175084HCID 22175084—
CatalystDimethylformamideHCID 6228—
SolventBenzeneHCID 241—
Product6-bromo-3-benzyloxy-4-methoxypyridine-2-carbonyl ChlorideHCID 22175073—

Reaction Steps

To a stirred mixture of 16 (2.54 g., 7.5 mmol) in benzene (30 mL) containing DMF (3 drops) was added oxalyl chloride (1.90 g, 15 mmol) in one portion. After gas evolution had ceased (about 45 min.), the now homogeneous solution was stirred an additional 15 min., then the solvent was evaporated. 1,2-dichloroethane (30 mL) was added and again the solvent was evaporated to give a quantitative yield of 3 as a nearly colorless oil. This material was dissolved in CH2Cl2 (10 mL) or THF (10 mL) and used directly in subsequent coupling reactions.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06521622B1
Source datasetuspto-grants-2003_02
ORD IDord-fbc29d051e034285b5f10d02ddd40e17
Source noteuspto-grants-2003_02