Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723479Generated: October 30, 2026

Triethylamine → (3S,4R)-1-tert-butyl 3-ethyl 4-(allyloxycarbonyl)piperidine-1,3-dicarboxylate

https://huagongshe.com/reaction/723479

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAllyl chloroformateHCID 18052—
Reactant1-tert-butyl 3-ethyl (3S,4R)-4-aminopiperidine-1,3-dicarboxylateHCID 58745494—
SolventDichloromethaneHCID 6344—
Product(3S,4R)-1-tert-butyl 3-ethyl 4-(allyloxycarbonyl)piperidine-1,3-dicarboxylateHCID 6695250160.4%

Reaction Steps

A solution of 259A (900 mg, 3.3 mmol) in CH2Cl2 (20 mL) was treated with triethylamine (0.64 mL, 4.62 mmol) and allylchloroformate (0.35 mL, 3.96 mmol) at room temperature. The mixture was stirred for four hours, then washed with 0.1 N HCl (2×10 mL), 1N NaOH (2×10 mL) and brine (10 mL). The organic layer was dried (Na2SO4), filtered and concentrated in vacuo to give 680 mg (yield: 58%) of Compound 259B as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141571B2
Source datasetuspto-grants-2006_11
ORD IDord-d342c7232c0e4ae19ccef030cad66712
Source noteuspto-grants-2006_11