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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729479Generated: October 31, 2026

Tetrahydrofuran → HCID 58367545, compound

https://huagongshe.com/reaction/729479

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant1-Bromo-2,4-difluorobenzeneHCID 67674—
ReactantTert-butyl 3-hydroxyazetidine-1-carboxylateHCID 2756801—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
ProductHCID 58367545HCID 58367545—

Reaction Steps

To a solution of Boc-3-hydroxyazetidine (1.50 g, 8.67 mmol) in DMF (9.1 mL) was added 1 M potassium tert-butoxide in THF (9.96 mL, 9.96 mmol) followed by 1-bromo-2,4-difluorobenzene (2.50 g, 13.0 mmol). After a period of 1 h at 50° C., the reaction mixture was partitioned between ethyl acetate and saturated ammonium chloride. The organic phase was separated, dried over sodium sulfate, filtered and evaporated under reduced pressure. The residue was purified by flash chromatography (15% ethyl acetate in hexane) to provide the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582633B2
Source datasetuspto-grants-2009_09
ORD IDord-54014c727c5346cba488ed09ec19cfb8
Source noteuspto-grants-2009_09