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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377547Generated: October 30, 2026

1,1'-Carbonyldiimidazole → N-(2,6-dihydroxyphenyl)-3-cyclopentyloxy-4-methoxyphenylacetamide

https://huagongshe.com/reaction/1377547

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant2-AminoresorcinolHCID 69451—
Reactant3-Cyclopentyloxy-4-methoxyphenylacetic acidHCID 10729342—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductN-(2,6-dihydroxyphenyl)-3-cyclopentyloxy-4-methoxyphenylacetamideHCID 2261829160%

Reaction Steps

A suspension of 3-cyclopentyloxy-4-methoxyphenylacetic acid (2.49 g) and 1,1'-carbonyldiimidazole (2.31 g) in dichloromethane (10 ml) was stirred at room temperature, under argon, for 2 hours. The resulting solution was added to a stirred suspension of 2-aminoresorcinol (1.62 g) in dichloromethane (15 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), 1N HCl (100 ml) and brine (100 ml), dried over CaSO4 and evaporated in-vacuo to yield the title compound (2.122 g, 60%) as a beige solid. δH (250MHz;d6DMSO) 1.53-1.95 (SH,m,4×CH2), 3.65 (2H, s,CH2), 3.70 (3H,s,OMe), 4.75 (1H,m, CH), 6.3 (1H,s,ArH), 6.35 (1H,s,ArH), 6.90 (4H,m,ArH), 9.40 (2H,s,ArOH), 9.6 (1H,s,CONH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665737
Source datasetuspto-grants-1997_09
ORD IDord-5ec2ccbd8c5a4d6f9eadd35a35f9f4d6
Source noteuspto-grants-1997_09