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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2362303Generated: November 2, 2026

Tetrahydrofuran → HCID 86678221, compound

https://huagongshe.com/reaction/2362303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactanto-Toluenesulfonyl chlorideHCID 8623—
ReactantSodium hydrideHCID 24758—
ReactantHCID 71293490HCID 71293490—
ProductHCID 86678221HCID 86678221—

Reaction Steps

Intermediate 22 (89 mg, 0.14 mmol) was dissolved in THF (3 ml), and then sodium hydride (6 mg, 0.2 mmol) was added under an atmosphere of N2. The reaction mixture was stirred at RT for 10 mins, then toluenesulfonyl chloride (31 mg, 0.16 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 yield the title compound as a colourless oil (70 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691826B2
Source datasetuspto-grants-2014_04
ORD IDord-0ce6c3cc73374c7ca1d439bc621c5d1b
Source noteuspto-grants-2014_04