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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1953232Generated: November 2, 2026

Ethyl propiolate → HCID 54535752, compound

https://huagongshe.com/reaction/1953232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl propiolateHCID 12182—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 54290816HCID 54290816—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 54535752HCID 5453575277.4%

Reaction Steps

To a mixture of 1-[4-(4-fluoro-phenoxy)-benzenesulfonylamino]-cyclopentanecarboxylic acid tert-butyl ester (1.0 g, 2.3 mmole) in 10 mL THF and 2.3 mL (2.3 mmole) 1M tetrabutylammonium fluoride in THF was added 0.23 mL (2.3 mmole) ethyl propiolate at ambient temperature. After stirring 1 hour the reaction was complete by HPLC and was stripped to dryness in vacuo. The residue was dissolved in 20 mL ethyl acetate and washed with 2×10 mL water and the organic solution stripped to an oil. This oil was chromatographed over silica gel, eluting with 10% ethyl acetate/hexane to yield 0.95 g (77% yield) 1-{(2-ethoxycarbonyl-vinyl)-[4-(4-fluoro-phenoxy)-benzenesulfonyl]-amino}-cyclopentanecarboxylic acid tert-butyl ester as a colorless oil. 1H NMR (CDCl3) indicated a 1.5:1 trans/cis ratio.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06114568
Source datasetuspto-grants-2000_09
ORD IDord-7e9d6960a11c4976aca8a4111095c0ca
Source noteuspto-grants-2000_09