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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1379354Generated: November 2, 2026

(3-Bromopropyl)benzene → HCID 22910127, compound

https://huagongshe.com/reaction/1379354

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-Bromopropyl)benzeneHCID 12503—
ReactantHCID 12701567HCID 12701567—
ReactantCID 53628100HCID 178418400—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22910127HCID 22910127—

Reaction Conditions

Temperature-25 °C

Reaction Steps

A solution of 1.0 g (4.2 mmol) of 2-(3-phenylpropyl)-1,3-dithiane in 25 ml of dry tetrahydrofuran was cooled to -78° C. and treated with 3.23 ml (4.2 mmol) of sec-butyllithium. The resulting solution was stirred at -25° C. for 20 min, recooled to -78° C., and treated with 0.64 ml (4.2 mmol) of 1-bromo-3-phenylpropane. After being stirred at -78° C. for 15 min, the solution was allowed to stir overnight at ambient temperature. The solution was partitioned between ether and aqueous ammonium chloride, and the organic layer was washed sequentially with water, 1M sodium bisulfite, and saturated brine, dried over MgSO4, and concentrated in vacuo to give the desired compound. 1H NMR (CDCl3) δ 1.65-1.9 (m, 9H), 2.18 (m, 1H), 2.55-2.75 (m, 6H), 2.78 (t, J=8 Hz, 1H), 3.40 (t, J=6 Hz, 1H), 7.1-7.35 (m, 10H). Mass spectrum (M+H)+ =357.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05670675
Source datasetuspto-grants-1997_09
ORD IDord-e2e0f575942747d4b5eaedbeb2b729b2
Source noteuspto-grants-1997_09