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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109864Generated: October 29, 2026

Benzyl Bromide → HCID 68832696, compound

https://huagongshe.com/reaction/2109864

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantHCID 68832620HCID 68832620—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68832696HCID 68832696—

Reaction Steps

To a solution of 5-acetyl-2-(4-fluorobenzyl)-7-(hydroxymethyl)-2,5-diazabicyclo[4.1.0]heptane-3-one (1.3 g, 4.45 mmol) in 40 mL anhydrous THF under nitrogen, sodium hydride (60% in mineral oil, 231 mg, 5.78 mmol) was added. After stirring for 1 h, benzyl bromide (0.58 ml, 4.89 mmol) in THF (1 mL) was added. The reaction mixture was stirred at room temperature overnight. The reaction was quenched with saturated aqueous ammonium chloride solution. The aqueous layer was extracted with chloroform three times. The combined organic phases were dried over sodium sulfate, filtered and concentrated. The residue was purified by column chromatography on silica gel using hexanes and ethyl acetate as eluents to give the title product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517532B2
Source datasetuspto-grants-2009_04
ORD IDord-1e04fd4c9ec1490da2a3faeb3a07d95c
Source noteuspto-grants-2009_04