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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1064381Generated: October 31, 2026

Benzyl Bromide → HCID 22273796, compound

https://huagongshe.com/reaction/1064381

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 22273744HCID 22273744—
SolventEthanolHCID 702—
ProductHCID 22273796HCID 2227379679.5%

Reaction Steps

600 mg (0.00165 mol) of (±)-1-hydroxy-7-[(4-phenylpiperidin-1-yl)carbonyl]-6,7,8,9-tetrahydro-5H-benzocyclohepten-5-one were dissolved in 100 mL of abs. EtOH under a nitrogen atmosphere, then 228 mg (0.00165 mol) of anhydrous K2CO3 and a catalytic amount of KI were added, followed by 0.216 mL (0.0018 mol) of benzylbromide. The reaction mixture was stirred 3 h at room temperature, then 0.216 mL of benzylbromide were added and the stirring continued overnight. Further 0.216 mL of benzylbromide was added and the reaction stirred overnight. The solvent was then evaporated, the residue was taken up in water, brought to pH 1 with 1N HCl and extracted with AcOEt. The organic phase was dried and the solvent was removed in vacuo, the resulting crude product was purified by flash chromatography, eluting with a mixture Et2O/Hexane 8:2 respectively, yielding 595 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06969724B2
Source datasetuspto-grants-2005_11
ORD IDord-b17f43ecdbfa40a8a37e8bf53f9a2627
Source noteuspto-grants-2005_11