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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1423304Generated: November 2, 2026

Ethanolamine → benzyl N-(2-hydroxyethyl)carbamate

https://huagongshe.com/reaction/1423304

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
ReactantBenzyl chloroformateHCID 10387—
SolventDichloromethaneHCID 6344—
Productbenzyl N-(2-hydroxyethyl)carbamateHCID 28045870%

Reaction Steps

To a stirred solution of ethanolamine (4.0 g, 66 mmol) in DCM (4 mL) was added benzyl chloroformate (4.6 mL, 33 mmol) at 0° C. After 1 h, the reaction mixture was warmed to room temperature and washed with 1.0N HCl (40 mL) and water (40 mL). The organics were separated, dried with anhydrous sodium sulfate, filtered, and concentrated. To a solution of the crude product in ethyl acetate (30 mL) was added hexanes (30 mL). The resulting crystals were filtered and dried to give the title intermediate as a white solid (4.5 g, 70%). 1H NMR (CDCl3, 300 MHz) δ (ppm): 7.4-7.29 (m, 5H), 5.00 (s, 2H), 4.64 (t, J=5.5 Hz, 1H), 3.38 (q, J=6.0 Hz, 2H), 3.07 (t, J=6.0 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927573B2
Source datasetuspto-grants-2015_01
ORD IDord-e1c17299b91340058a940b530cec922f
Source noteuspto-grants-2015_01