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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 425080Generated: October 25, 2026

Sodium hydride → HCID 66704611, compound

https://huagongshe.com/reaction/425080

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant(-)-3-HydroxytetrahydrofuranHCID 641512—
ReactantHCID 59557747HCID 59557747—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66704611HCID 6670461180%

Reaction Steps

To a stirred solution of (R)-tetrahydrofuran-3-ol (320 mg, 3.63 mmol) in dry tetrahydrofuran (10 mL) was added sodium hydride (145 mg, 3.63 mmol, 60%) slowly under 0° C. The reaction was stirred at this temperature for 30 min and then 2-(4-(5-bromo-2-chlorobenzyl)phenoxy)ethyl 4-methylbenzenesulfonate (intermediate AB) (300 mg, 0.61 mmol) was added. The reaction was warmed to room temperature and then heated to reflux overnight. The reaction was quenched with saturated ammonium chloride and extracted with ethyl acetate. The organic layer was washed with brine, dried over sodium sulfate and concentrated to a yellow oil. The crude oil was purified by flash chromatography to get 200 mg of colorless oil (80% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106021B2
Source datasetuspto-grants-2012_01
ORD IDord-13d2b61fe8d64769908f235f01fb2284
Source noteuspto-grants-2012_01