Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570876Generated: October 30, 2026

Tetrahydrofuran → HCID 86678221, compound

https://huagongshe.com/reaction/570876

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 eluding 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 numberUS09023855B2
Source datasetuspto-grants-2015_05
ORD IDord-7d7921b9083c4fb2a27e6274ff6fc311
Source noteuspto-grants-2015_05