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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1697623Generated: October 31, 2026

2-Chloroethanol → 2-(4-Bromo-phenyl)-[1,3]dioxolane-2-carboxylic Acid Ethyl Ester

https://huagongshe.com/reaction/1697623

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloroethanolHCID 34—
ReactantTetrahydrofuranHCID 8028—
ReactantEthyl 2-(4-bromophenyl)-2-oxoacetateHCID 10729811—
ReactantPotassium tert-butoxideHCID 86639980—
SolventDimethylformamideHCID 6228—
Product2-(4-Bromo-phenyl)-[1,3]dioxolane-2-carboxylic Acid Ethyl EsterHCID 6677204658%

Reaction Conditions

Temperature-60 °C

Reaction Steps

To a solution of ethyl-4-bromobenzoylformate (940 mg) and 2-chloroethanol (0.360 mL) in a 2:1 mixture of dimethylformamide:tetrahydrofuran (2.1 mL) was added dropwise at −60° C. a solution of potassium tert-butanol (0.597 mg) in dimethylformamide (2 mL). The reaction mixture was stirred at −60° C. for 4 h then allowed to warm up to room temperature and stirred at room temperature overnight. The reaction mixture was partitioned between an aqueous solution of ammonium chloride and ethyl acetate. The aqueous layer was extracted with ethyl acetate and the combined organic layer were washed with brine. The crude mixture was concentrated to dryness and purified by chromatography on silica gel to yield the title compound as a colorless liquid (616 mg; 58%). MS (ESI): m/z=300.8 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163793B2
Source datasetuspto-grants-2012_04
ORD IDord-7fb622fe119b449c9486b2338dee5d13
Source noteuspto-grants-2012_04