Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1843284Generated: November 3, 2026

Triethylamine → 1-Benzyl-1,2,3,4-tetrahydroquinolin-7-yl 2-methylphenylcarbamate

https://huagongshe.com/reaction/1843284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Tolyl isocyanateHCID 69194—
Reactant1-Benzyl-1,2,3,4-tetrahydroquinolin-7-olHCID 21864936—
SolventDichloromethaneHCID 6344—
Product1-Benzyl-1,2,3,4-tetrahydroquinolin-7-yl 2-methylphenylcarbamateHCID 60163390—

Reaction Conditions

Temperature35 °C

Reaction Steps

A mixture of 1-benzyl-1,2,3,4-tetrahydroquinolin-7-ol (550 mg, 2.30 mM) and triethylamine (0.4 mL) in dry dichloromethane (DCM, 10 mL) was stirred for half an hour under nitrogen atmosphere at room temperature (35° C.). To the stirred reaction mixture, o-tolyl isocyanate (428 mg/ml, 3.45 mM) was added at once and then the reaction mixture was further stirred for 72 hours under N2 atmosphere at RT. The reaction mixture was concentrated under vacuum and then was added distilled water (15 mL) followed by the extraction with ether (3×15 mL). The ether layer was dried over sodium sulphate and concentrated under vacuum to afford the crude product, which was finally chromatographed using chloroform-hexane (1:9) to give 8a as colorless oil. Yield: 700 mg, 81.78%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946261B2
Source datasetuspto-grants-2015_02
ORD IDord-51bf201873664e67ba6a1250fb409bbc
Source noteuspto-grants-2015_02