HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 365856Generated: October 25, 2026
4-Vinylpyridine → HCID 54034311, compound
https://huagongshe.com/reaction/365856
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Vinylpyridine | HCID 7502 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Reactant | 3-bromo-5-[[1-(tert-butoxycarbonyl)-2(R)-pyrrolidinyl]methoxy]pyridine | HCID 15480236 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 54034311 | HCID 54034311 | 79% |
Reaction Steps
A mixture of 5-bromo-3-(1-BOC-2-(R)-pyrrolidinylmethoxy)pyridine (440 mg, 1.25 mmol), 4-vinylpyridine (0.267 mL), Pd(OAc)4 (30 mg), tris(o-tolyl)phosphine (160 mg), and triethylamine (3.5 mL) in acetonitrile (4 mL) was heated at reflux for 16 hours. The solution was then concentrated, and the residue was washed with water and aqueous NaHCO3 solution. The organic layer was dried and concentrated. The residue was chromatographed on a silica gel column, eluting with hexane:EtOAc 1:3 to afford the title compound (440 mg, 79% yield). MS (CI/NH3) m/z 382 (M+H)+. 1H NMR (CDCl3, 300 MHz) δ1.49 (s, 3H), 1.85-2.12 (m, 4H), 3/26 -3.55 (m, 2H), 3.86-4.08 (m, 1H), 4.08--4.34 (m, 1H), 7.20-7.30 (m, 2H), 7.36-7.42 (m, 2H), 7.71 (br s, 0.5 H), 8.22-8.42 (m, 1.5 H), 8.58-8.69 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06127386 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-77a8f99e9e7a41c09a8bb7a3d74b0850 |
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| Source note | uspto-grants-2000_10 |
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