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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487215Generated: October 30, 2026

Benzyl Bromide → Benzyl 6,7-dichloro-4H-1-benzopyran-4-carboxylate

https://huagongshe.com/reaction/487215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium BicarbonateHCID 516892—
Reactant6,7-dichloro-4H-1-benzopyran-4-carboxylic acidHCID 14986561—
SolventDichloromethaneHCID 6344—
ProductBenzyl 6,7-dichloro-4H-1-benzopyran-4-carboxylateHCID 19094451—

Reaction Steps

A mixture of 6,7-dichloro-4H-1-benzopyran-4-carboxylic acid (16.8 gm), tetra (N-butyl)ammonium hydrogensulfate (23 gm), benzyl bromide (9.7 mL), saturated sodium bicarbonate (100 mL) and dichloromethane (100 mL) were stirred vigorously at room temperature for 14 hours, then diluted with dichloromethane, and the organic layer separated, washed with saturated sodium bicarbonate, water, brine, dried (MgSO4), filtered and evaporated. The residue was purified by column chromatography (2:1 dichloromethane/hexanes, SiO2) to afford the title compound (11.8 gm, Rf=0.3 (2:1 dichloromethane/hexanes, SiO2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05294635
Source datasetuspto-grants-1994_03
ORD IDord-2173650d53ea4f079ddc1f7e2ac811d0
Source noteuspto-grants-1994_03