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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842094Generated: October 31, 2026

1,1'-Carbonyldiimidazole → N-(2-hydroxy-3-nitrophenyl)-3-cyclopentyloxy-4-methoxyphenylacetamide

https://huagongshe.com/reaction/842094

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant2-Amino-6-nitrophenolHCID 5127291—
Reactant3-Cyclopentyloxy-4-methoxyphenylacetic acidHCID 10729342—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductN-(2-hydroxy-3-nitrophenyl)-3-cyclopentyloxy-4-methoxyphenylacetamideHCID 2261827868%

Reaction Steps

A suspension of 3-cyclopentyloxy-4-methoxyphenylacetic acid (1.00 g) and 1,1′-carbonyl diimidazole (821 mg) in dichloromethane (5 ml) was stirred at room temperature, under argon, for 2 hours. The resulting solution was added to a stirred solution of 2-amino-6-nitrophenol (723 mg) in dichloromethane (10 ml) and the mixture stirred at room temperature, under argon, overnight. The reaction mixture was diluted with water (100 ml) and extracted with dichloromethane (3×50 ml). The combined organic extracts were washed with water (100 ml), 1 N HCl (50 ml) and brine (50 ml), dried over CaSO4 and evaporated in-vacuo to yield the title compound (1.05 g, 68%) as an orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06372770B1
Source datasetuspto-grants-2002_04
ORD IDord-5abd6d711a424e84975c7298d7e8a334
Source noteuspto-grants-2002_04