Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079382Generated: October 31, 2026

Triethylamine → HCID 58010986, compound

https://huagongshe.com/reaction/2079382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Methoxyethyl chloroformateHCID 69400—
Reactanttert-Butyl (3S)-3-(aminomethyl)piperidine-1-carboxylateHCID 1502022—
SolventDichloromethaneHCID 6344—
ProductHCID 58010986HCID 5801098667.3%

Reaction Steps

To a solution of (S)-tert-butyl 3-(aminomethyl)piperidine-1-carboxylate (500 mg, 2.33 mmol) in CH2Cl2 at −10° C. was added triethylamine (650 μL, 4.66 mmol) followed by the dropwise addition of 2-methoxyethyl chloroformate (325 μL, 2.79 mmol). The reaction was warmed to room temperature and quenched with water. The aqueous layer was extracted with CH2Cl2, and the combined extracts were dried over MgSO4, filtered, and evaporated. Purification via silica gel chromatography using 0 to 10% EtOAc in CH2Cl2 afforded 2-methoxyethyl ((S)-1-(tert-butoxycarbonyl)piperidin-3-yl)methylcarbamate (496 mg, 67%). LC/MS: m/z 317.3 (M+H)+ at 2.56 min (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928107B2
Source datasetuspto-grants-2011_04
ORD IDord-431b4a188e01487eba46f822c92bd750
Source noteuspto-grants-2011_04