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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55752Generated: October 25, 2026

Oxalyl chloride → 6-Bromo-2-naphthoyl chloride

https://huagongshe.com/reaction/55752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant6-Bromo-2-naphthalenecarboxylic acidHCID 4549852—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product6-Bromo-2-naphthoyl chlorideHCID 21879606100.1%

Reaction Steps

6-bromo-2-naphthoic acid (72.3 g, 282 mmol, 1.0 equiv.) was suspended in dichloromethane (600 mL) and DMF (catalytic, 5 drops) was added. Oxalylchloride (71.6 g, 564 mmol, 2.0 equiv.) was added portion wise during 1 hour. The reaction mixture was stirred overnight with a CaCl2 drying tube mouthed on the flask. Complete dissolution occurred. The reaction mixture was concentrated, dichloromethane (100 mL) was added and the solvent was evaporated again, yielding 6-bromo-2-naphthoyl chloride (76.1 g, 100%) as an oil which was used as such in next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09433609B2
Source datasetuspto-grants-2016_09
ORD IDord-8e890819485b476c9aa40cc3b93e3f03
Source noteuspto-grants-2016_09