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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666314Generated: November 1, 2026

1,1'-Carbonyldiimidazole → 2-(3,4,5-trimethoxyphenyl)-2-acetoxy-N-methyl-N-[1-(3-methoxyphenyl)ethyl]acetamide

https://huagongshe.com/reaction/1666314

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant1-(3-Methoxyphenyl)-N-methylethanamineHCID 14871688—
Reactantalpha-Acetoxy-3,4,5-trimethoxyphenyl-acetic acidHCID 67081678—
SolventDichloromethaneHCID 6344—
Product2-(3,4,5-trimethoxyphenyl)-2-acetoxy-N-methyl-N-[1-(3-methoxyphenyl)ethyl]acetamideHCID 6708183667.5%

Reaction Steps

A solution of α-acetoxy-3,4,5-trimethoxyphenyl-acetic acid (7.1 g) in dichloromethane (50 ml) was reacted with 1,1′-carbonyldiimidazole (4.06 g) at room temperature for 30 minutes. The solution was refluxed for 30 minutes, after which 1-(3-methoxyphenyl)-N-methylethylamine (4.13 g) dissolved in dichloromethane (10 ml) was added. The mixture was stirred at room temperature for 2 hours, after which it was washed with aqueous hydrochloric acid (20 ml, 1M) followed by aqueous sodium hydrogen carbonate (20 ml, 0.5 M). The organic phase was dried and concentrated to dryness, leaving crude 2-(3,4,5-trimethoxyphenyl)-2-acetoxy-N-methyl-N-[1-(3-methoxyphenyl)ethyl]acetamide (7.27 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044067B2
Source datasetuspto-grants-2011_10
ORD IDord-f32053fd8ae94d6d818fe6f4e0d4de44
Source noteuspto-grants-2011_10