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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantMethyl 1-Benzyl-1,2,3,6-tetrahydropyridine-4-carboxylateHCID 21764251—
ReactantHCID 178419620HCID 178419620—
SolventTolueneHCID 1140—
ProductMethyl 1-benzyl-3-(3-bromophenyl)piperidine-4-carboxylateHCID 6850407960.5%

Reaction Conditions

Temperature20 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795436B2
Source datasetuspto-grants-2010_09
ORD IDord-15c39f80fdea4bae98202778e2fd0952
Source noteuspto-grants-2010_09