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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417314Generated: November 2, 2026

Hydrochloric Acid → Ethyl(1RS,5RS,6RS)-6-fluoro-2-oxobicyclo[3.1.0]hexane-6-carboxylate

https://huagongshe.com/reaction/2417314

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodoethaneHCID 6340—
ReactantSodium BicarbonateHCID 516892—
Reactant6-Fluoro-2-oxobicyclo[3.1.0]hexane-6-carboxylic acidHCID 22634779—
SolventDimethylformamideHCID 6228—
ProductEthyl(1RS,5RS,6RS)-6-fluoro-2-oxobicyclo[3.1.0]hexane-6-carboxylateHCID 9964278—

Reaction Conditions

Temperature50 °C

Reaction Steps

(1RS,5RS,6RS)-6-fluoro-2-oxobicyclo[3.1.0]hexane-6-carboxylic acid in an amount of 1.0 g was dissolved in 5.0 mL of N,N-dimethylformamide, and 0.58 g of sodium hydrogencarbonate and 1.5 mL of ethyl iodide were added thereto. The mixture was stirred overnight at 50° C. The reaction mixture was poured into 1M hydrochloric acid, followed by extractions with ethyl acetate three times. The organic layer was dried over anhydrous sodium sulfate. After the desiccant was filtered off, the filtrate was concentrated under reduced pressure. The residue was purified by column chromatography (silica gel: Wako gel C200 (produced by Wako Pure Chemical Industries Ltd.), eluent: hexane-ethyl acetate=8:1), thereby yielding 1.1 g of (1RS,5RS,6RS)ethyl 6-fluoro-2-oxobicyclo[3.1.0]hexane-6-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06825375B2
Source datasetuspto-grants-2004_11
ORD IDord-9ad01512c32049beb83c03d2a4793c32
Source noteuspto-grants-2004_11