Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270767Generated: October 25, 2026

Ethanol → N-(6-fluoro-2-naphthyl)carbamic acid ethyl ester

https://huagongshe.com/reaction/1270767

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant6-Fluoro-2-naphthoic acidHCID 2782788—
Solvent1,4-DioxaneHCID 31275—
ProductN-(6-fluoro-2-naphthyl)carbamic acid ethyl esterHCID 68804469—

Reaction Steps

To a suspension of 6-fluoro-2-naphthoic acid (450 mg, 2.37 mmol) and triethylamine (0.66 mL, 4.73 mmol) in 1,4-dioxane (30 mL) at room temperature, is added DPPA (0.77 mL, 3.55 mmol). After stirring at room temperature for 2.5 hours, ethanol (1.38 mL, 23.7 mmol) is added and the reaction is heated to reflux temperature for 12 hours. After cooling to room temperature, the mixture is partitioned between EtOAc and water. The organic layer is washed with brine, dried (Na2SO4) and concentrated by rotary evaporator to give an oil. Flash chromatography on silica gel (3:1 hexanes/EtOAc) gives N-(6-fluoro-2-naphthyl)carbamic acid ethyl ester as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07202364B2
Source datasetuspto-grants-2007_04
ORD IDord-9889c43ee7a0494f9237e9f5a932a7c9
Source noteuspto-grants-2007_04