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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2275730Generated: October 31, 2026

Hydrochloric Acid → HCID 66961506, compound

https://huagongshe.com/reaction/2275730

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzeneacetic acid, 4-bromo-HCID 74654—
ReactantLithium diisopropylamideHCID 2724682—
Reactant(2-Bromoethoxy)-tert-butyldimethylsilaneHCID 3608067—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66961506HCID 6696150619%

Reaction Conditions

Temperature-78 °C

Reaction Steps

4-Bromophenylacetic acid (1.00 g, 4.65 mmol) was dissolved in 45 mls of dry THF and chilled to −78° C. To this was added LDA (9.30 mls, 18.6 mmol, 2M in THF/heptane), resulting in a dark color, and this mixture was stirred at −78° C. for 20 minutes. (2-bromoethoxy)(tert-butyl)dimethylsilane (1.20 mls, 5.58 mmol) was then added via syringe, and then the cooling bath was removed to allowed the reaction to warm to room temperature. Upon warming, the mixture became an amber color. Once at room temperature, 50 mls of 1N aqueous HCl were then added and the mixture was vigorously stirred for 16 hours, then extracted with EtOAc (2×), extracts washed with 2M aqueous sodium carbonate, dried over sodium sulfate and concentrated to an orange oil. Flash 40 Biotage (40M cartridge, 3:1 Hexane:EtOAc) afforded 211 mgs (19%) of 3-(4-bromophenyl)dihydrofuran-2(3H)-one as an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126940B2
Source datasetuspto-grants-2015_09
ORD IDord-060c730a349e47ebad52189bb945ce6c
Source noteuspto-grants-2015_09