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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570880Generated: October 29, 2026

Tetrahydrofuran → HCID 86678224, compound

https://huagongshe.com/reaction/570880

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactanto-Toluenesulfonyl chlorideHCID 8623—
ReactantSodium hydrideHCID 24758—
ReactantHCID 71293508HCID 71293508—
ProductHCID 86678224HCID 86678224—

Reaction Steps

Intermediate 28 (470 mg, 0.76 mmol) was dissolved in THF (5 ml), and then sodium hydride (48 mg, 1.2 mmol) was added under an atmosphere of N2. The reaction mixture was stirred at RT for 10 mins, then toluenesulfonyl chloride (191 mg, 1 mmol) was added and stirring was continued for 16 hours. The reaction mixture was partitioned between EtOAc and water. The organic layer was separated, washed with brine, dried (Na2SO4) and evaporated in vacuo. The resulting residue was purified by silica gel chromatography Bluing with a gradient of 50-80% EtOAc in cyclohexane to give the title compound as a pale yellow glass (132 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09023855B2
Source datasetuspto-grants-2015_05
ORD IDord-4198cc1b4bbf4947a74af796854f6bdc
Source noteuspto-grants-2015_05