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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270771Generated: November 2, 2026

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

https://huagongshe.com/reaction/1270771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant6-Chloronaphthalene-2-carboxylic acidHCID 13288327—
Solvent1,4-DioxaneHCID 31275—
ProductN-(6-chloro-2-naphthyl)carbamic acid ethyl esterHCID 68803058—

Reaction Steps

To a suspension of 6-chloro-2-naphthoic acid (1 g, 4.84 mmol) and triethylamine (1.35 mL, 9.68 mmol) in 1,4-dioxane (20 mL) at room temperature, is added DPPA (1.56 mL, 7.26 mmol). After stirring at room temperature for 2.5 hours, ethanol (2.82 mL, 48.4 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-chloro-2-naphthyl)carbamic acid ethyl ester as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07202364B2
Source datasetuspto-grants-2007_04
ORD IDord-761ed3b65c7a4ce99bfd4fb4449fbdcb
Source noteuspto-grants-2007_04