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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1064384Generated: October 30, 2026

Allyl bromide → HCID 69802498, compound

https://huagongshe.com/reaction/1064384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantSodium hydrideHCID 24758—
ReactantEther hydrochlorideHCID 10953452—
ReactantHCID 69799954HCID 69799954—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69802498HCID 69802498—

Reaction Steps

0.2 g (0.596 mmol) of (±)-cis-7-[(4-phenylpiperdin-1-yl)methyl]-6,7,8,9-tetrahydro-5H-benzocyclohepten-5-ol dissolved in 5 ML THF were added dropwise to a suspension of 0.029 g (0.715 mmol) of NaH (60% dispersion in mineral oil) in 10 mL THF. After 30 min at room temperature, 0.12 mL of allyl bromide were added and the reaction mixture was refluxed 8 h. After cooling, the reaction mixture was quenched by addition of MeOH and the solvent was removed in vacuo. The residue was taken up in 1 N NaOH and extracted with CH2Cl2; the organic phase was dried and the solvent was removed in vacuo. The resulting crude product was purified by chromatography, eluting with a mixture CH2Cl2/MeOH 100:2 respectively, yielding an oil which was dissolved in Et2O; the solution was brought to acidic pH with Et2O/HCl and the solvent was removed in vacuo. The resulting solid was triturated with Et2O, yielding 65 mg of the title product. m.p. 126-128° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06969724B2
Source datasetuspto-grants-2005_11
ORD IDord-53ab4c17a69d44548ca8bd3dcade4296
Source noteuspto-grants-2005_11