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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403759Generated: October 31, 2026

Sodium hydride → HCID 59557738, compound

https://huagongshe.com/reaction/2403759

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantCyclobutanolHCID 76218—
Reactant2-(4-(5-Bromo-2-chlorobenzyl)phenoxy)ethyl 4-methylbenzenesulfonateHCID 59557747—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59557738HCID 5955773849.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of cyclobutanol (260 mg, 3.6 mmol) in anhydrous tetrahydrofuran (4 mL) was added sodium hydride (138 mg, 5.7 mmol) in portions at 0° C. The mixture was stirred at 0° C. for 30 min, and then 2-(4-(5-bromo-2-chlorobenzyl)phenoxy)ethyl 4-methylbenzenesulfonate (intermediate AB) (300 mg, 0.6 mmol) was added in portions. The mixture was refluxed for 3 h, whereupon TLC showed the reaction was complete. The reaction mixture was quenched with saturated ammonium chloride, extracted with ethyl acetate, washed with water and then with brine, dried over anhydrous sodium sulfate, and concentrated to a crude oil. The crude oil was purified by column chromatography (PE:EA=10:1) to get intermediate CL as an oil product (117 mg, yield: ˜49%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802637B2
Source datasetuspto-grants-2014_08
ORD IDord-865e0d513a33441ba1d021aa0d53b28c
Source noteuspto-grants-2014_08