Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723474Generated: October 29, 2026

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

https://huagongshe.com/reaction/723474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant(3R,4R)-1-tert-butyl 3-ethyl 4-aminopiperidine-1,3-dicarboxylateHCID 58745614—
SolventDichloromethaneHCID 6344—
Product(3R,4R)-1-tert-butyl 3-ethyl 4-(benzyloxycarbonyl)piperidine-1,3-dicarboxylateHCID 66952821188.1%

Reaction Steps

A solution of 252E (180 mg, 0.66 mmol) in CH2Cl2 (5 mL) was treated with benzyloxychloroformate (0.1 mL, 0.73 mmol) and triethylamine (0.12 mL, 0.86 mmol). The reaction was stirred at room temperature for 18 hours, diluted with CH2Cl2 (10 mL) and washed with water (2×10 mL), 0.1 N HCl (2×10 mL), saturated aqueous NaHCO3 (2×10 mL) and brine (1×10 mL). The organic layer was dried (Na2SO4), filtered and concentrated to give 243 mg (yield: 91%) of Compound 254A as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141571B2
Source datasetuspto-grants-2006_11
ORD IDord-dc360af6e8cf437ea52755a44f1fd2bc
Source noteuspto-grants-2006_11