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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1843286Generated: November 1, 2026

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

https://huagongshe.com/reaction/1843286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Fluorophenyl isocyanateHCID 85588—
Reactant1-Benzyl-1,2,3,4-tetrahydroquinolin-7-olHCID 21864936—
SolventTetrahydrofuranHCID 8028—
Product1-Benzyl-1,2,3,4-tetrahydroquinolin-7-yl 2-fluorophenylcarbamateHCID 60163506—

Reaction Conditions

Temperature35 °C

Reaction Steps

A mixture of 1-benzyl-1,2,3,4-tetrahydroquinolin-7-ol (805 mg, 3.36 mM) and triethylamine (0.6 mL) in dry tetrahydrofuran (THF, 5 ml) was stirred for half an hour under nitrogen atmosphere at room temperature (35° C.). To the stirred reaction mixture, 2-fluorophenyl isocyanate (565 mg/ml, 5.04 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 8c as oil. Yield: 1.02 g, 80.56%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946261B2
Source datasetuspto-grants-2015_02
ORD IDord-67b555340d0f4b5e8e3b126b1eee5e6a
Source noteuspto-grants-2015_02