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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425043Generated: November 2, 2026

Hydrochloric Acid → HCID 11380123, compound

https://huagongshe.com/reaction/2425043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Cyclopenten-1-oneHCID 13588—
ReactantChlorotriethylsilaneHCID 13819—
ReactantEthyl 2,2-dibromo-2-fluoroacetateHCID 2737168—
CatalystZincHCID 23994—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 11380123HCID 1138012388%

Reaction Steps

Add 8.45 mL (50.4 mmol) of triethylsilyl chloride to a suspension of 2.99 g of activated Zn (45.8 mmol) in anhydrous acetonitrile (100 mL) at −20° C. and stir the mixture for 5 minutes. Add 8.0 mL (57.3 mmol) of ethyl 2,2-dibromo-2-fluoracetate and stir the mixture for 90 minutes at −20° C. Add 1.86 mL (22.9 mmol) of 2-cyclopenten-1-one, and stir the reaction mixture overnight, allowing the temperature to rise slowly to room temperature. Add HCl 1N (125 mL) and EtOAc (100 mL). Wash the organic layer with saturated NaHCO3 (2×150 mL), water (2×150 mL) and brine (2×150 mL), dry over anhydrous MgSO4, filter and concentrate under reduced pressure. Purify the residue by column chromatography using EtOAc/hexane (1:8) as eluent to give the title compound (5.36 g, 88% overall yield) as a colorless oil as a mixture of diastereoisomers.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07964632B2
Source datasetuspto-grants-2011_06
ORD IDord-6822f75de1de42c3b711b8979bc8e151
Source noteuspto-grants-2011_06