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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615072Generated: October 30, 2026

Water → HCID 59633945, compound

https://huagongshe.com/reaction/1615072

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-Oxo-azetidine-1-carboxylic acid tert-butyl esterHCID 1519404—
ReactantHCID 59633897HCID 59633897—
ReactantHCID 178418244HCID 178418244—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59633945HCID 5963394557%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 4-bromo-1-(4-ethylbenzyloxy)-2-methoxybenzene (1.2 g) prepared in (1) in THF (6.0 mL) was added dropwise 1.6 N n-butyllithium/hexane (2.8 mL) at −78° C. under argon atmosphere. The mixture was stirred at −78° C. for 30 min. A solution of 1-Boc-azetidin-3-one (0.64 g) in THF (6.0 mL) was added dropwise over 10 min to the mixture at −78° C. The reaction mixture was allowed to warm to RT and then stirred for 14 hr. Water was added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was dried over MgSO4. The solvent was removed under reduced pressure. The residue was purified by silica gel chromatography (Developing solvent: hexane/ethyl acetate=3/1 to 1/1) to give the title compound (0.88 g, 57%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765739B2
Source datasetuspto-grants-2014_07
ORD IDord-13ad4f11d18d4a96a1b12c8273acc938
Source noteuspto-grants-2014_07