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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1976768Generated: October 25, 2026

Triethylamine → N-(2-hydroxy-2-phenylethyl)-3,5-dimethoxybenzamide

https://huagongshe.com/reaction/1976768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3,5-Dimethoxybenzoic AcidHCID 14332—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant2-Amino-1-(3,4,5-trimethoxyphenyl)ethanolHCID 28894—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
SolventDichloromethaneHCID 6344—
ProductN-(2-hydroxy-2-phenylethyl)-3,5-dimethoxybenzamideHCID 2199872294.3%

Reaction Steps

A suspension of 3,5-dimethoxybenzoic acid (1.00 g, 5.49 mmol) in dichloromethane (50 mL) at 0° C. was treated with HOBt hydrate (0.742 g, 5.49 mmol), stirred for 15 minutes, treated with EDCI (1.05 g, 5.49 mmol) in one portion, stirred for an additional 25 minutes, treated with triethylamine (1.84 g; 2.53 mL, 1.9 mmol) and the acetate salt of 2-amino-1-(3,4,5-trimethoxyphenyl)ethanol (1.58 g, 005.49 mmol), stirred for 18 hours while warming to room temperature, and concentrated. The concentrate was partitioned between ethyl acetate (400 mL) and water (200 mL), and the organic extract was washed sequentially with 10% KHSO4 (200 mL), water (100 mL), NaHCO3 (200 mL), and water (100 mL), dried (MgSO4), filtered, and concentrated to provide 1.56 g of the desired product as a white foamy semi-solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06228868B1
Source datasetuspto-grants-2001_05
ORD IDord-36ba17b6e39a493ba227457f28b989b9
Source noteuspto-grants-2001_05