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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1856817Generated: November 2, 2026

Tetrahydrofuran → 5-Ethoxycarbonylamino-2-(3,3,3-trifluoropropyl)-benzofuran

https://huagongshe.com/reaction/1856817

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantEthyl chloroformateHCID 10928—
ReactantSodium BicarbonateHCID 516892—
Reactant5-Amino-2-(3,3,3-trifluoropropyl)benzofuranHCID 22132957—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product5-Ethoxycarbonylamino-2-(3,3,3-trifluoropropyl)-benzofuranHCID 1113039795.4%

Reaction Steps

A solution of 2.0 g (8.7 mmol) of 5-amino-2-(3,3,3-trifluoropropyl) benzofuran in 30 ml of a 9/1 mixture of tetrahydrofuran and water is reacted for 30 min with 0.92 ml (9.6 mmol) of ethyl chloroformate in the presence of 1.1 g (13 mmol) of sodium hydrogen-carbonate. The reaction mixture is then diluted with water and dichloromethane, and then the organic phase is separated, dried over sodium sulfate and concentrated under reduced pressure. 2.5 g of product are obtained. Melting point: 108° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06143772
Source datasetuspto-grants-2000_11
ORD IDord-3ca35e2895014cfba8cf76a6e1828cd2
Source noteuspto-grants-2000_11