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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 645303Generated: October 31, 2026

2,3-Dihydrofuran → HCID 66735283, compound

https://huagongshe.com/reaction/645303

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-DihydrofuranHCID 70934—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 66735592HCID 66735592—
SolventDichloromethaneHCID 6344—
ProductHCID 66735283HCID 6673528340.7%

Reaction Steps

To a solution of 0.25 g of 4-(3-(3,5-dichlorophenyl)-4,4,4-trifluoro-2-butenoyl)benzoic acid amide that was synthesized under Synthetic Example 9 in 3 mL of dichloromethane, 68 mg of 2,3-dihydrofuran and a catalytic amount of p-toluenesulfonic acid monohydrate were added and the mixture was stirred for 18 hours at room temperature. The solvent was distilled off from the reaction solution under reduced pressure, and the resulting residue was purified using silica gel column chromatography that was eluted with ethyl acetate-hexane (2:3) followed by crystallization from a mixed solvent of hexane and a small amount of ethyl acetate to obtain 0.12 g of aimed product as yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700808B2
Source datasetuspto-grants-2010_04
ORD IDord-54e0e0e88d89496ea2a66552cf447732
Source noteuspto-grants-2010_04