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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2362307Generated: November 1, 2026

Tetrahydrofuran → HCID 86678224, compound

https://huagongshe.com/reaction/2362307

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 eluing 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 numberUS08691826B2
Source datasetuspto-grants-2014_04
ORD IDord-d42d1a58d2d2445da9eda0344bccbe10
Source noteuspto-grants-2014_04