HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714131Generated: November 3, 2026
Tetrahydrofuran → Methyl 1-benzyl-3-(3-bromophenyl)piperidine-4-carboxylate
https://huagongshe.com/reaction/1714131
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Methyl 1-Benzyl-1,2,3,6-tetrahydropyridine-4-carboxylate | HCID 21764251 | — |
| Reactant | HCID 178419620 | HCID 178419620 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Methyl 1-benzyl-3-(3-bromophenyl)piperidine-4-carboxylate | HCID 68504079 | 60.5% |
Reaction Steps
A 0.5 M THF solution of (3-bromophenyl)magnesium bromide (20 mL, 10 mmol) was cooled to −15° C., and methyl 1-benzyl-1,2,3,6-tetrahydropyridine-4-carboxylate (1.05 g, 4.3 mmol) in toluene (3.0 mL) was slowly added for 3 h at −15° C. The reaction mixture was warmed to 20° C. and quenched by addition of saturated NH4Cl aqueous solution followed by extraction with EtOAc. The combined organic solution was dried over MgSO4, filtered and concentrated in vacuo. The residue was chromatographed in silica gel column (Hex/EtOAc 9/1) to give methyl 1-benzyl-3-(3-bromophenyl)piperidine-4-carboxylate (1.0 g, 2.6 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07795436B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-15c39f80fdea4bae98202778e2fd0952 |
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| Source note | uspto-grants-2010_09 |
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