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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1866716Generated: October 26, 2026

Diisopropylethylamine → 1-Benzyl 4-methyl 4-allylpiperidine-1,4-dicarboxylate

https://huagongshe.com/reaction/1866716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzyl succinimido carbonateHCID 83172—
ReactantMethyl 4-allylpiperidine-4-carboxylateHCID 66972977—
SolventAcetonitrileHCID 6342—
Product1-Benzyl 4-methyl 4-allylpiperidine-1,4-dicarboxylateHCID 58893186—

Reaction Steps

A mixture of methyl 4-allylpiperidine-4-carboxylate from Step A (5.30 g, 24.2 mmol), N-(benzyloxycarbonyloxy)succinimide (7.25 g, 29.1 mmol), and N,N-diisopropylethylamine (12.7 mL, 72.7 mmol) in CH3CN (61 mL) was stirred for 16 h. The solvent was removed in vacuo and the residue was partitioned between EtOAc (100 mL) and saturated NaHCO3 (100 mL). The organic layer was separated and the aqueous layer was further extracted with EtOAc (2×100 mL).The combined organic extracts were concentrated in vacuo to give a residue that was purified by silica gel chromatography, eluting with a gradient of hexane:EtOAc—100:0 to 40:60, to give the title compound. MS: m/z=318 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07629338B2
Source datasetuspto-grants-2009_12
ORD IDord-7fdec9052108494e939c6d1e0c4836dc
Source noteuspto-grants-2009_12