HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847601Generated: October 30, 2026
(3-Bromopropyl)benzene → HCID 22910127, compound
https://huagongshe.com/reaction/847601
Participants
| Role | Name | HCID | Charge |
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| Reactant | (3-Bromopropyl)benzene | HCID 12503 | — |
| Reactant | HCID 12701567 | HCID 12701567 | — |
| Reactant | CID 53628100 | HCID 178418400 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22910127 | HCID 22910127 | — |
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 secbutyllithium. 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, 1 M sodium bisulfite, and saturated brine, dried over MgSO4, and concentrated in vacuo to give the desired compound. 1H NMR (CDCl3) δ 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05142056 |
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| Source dataset | uspto-grants-1992_08 |
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| ORD ID | ord-75087601769346d3aef001d3e13424c0 |
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| Source note | uspto-grants-1992_08 |
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