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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3,5-Dimethoxybenzoic Acid | HCID 14332 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 2-Amino-1-(3,4,5-trimethoxyphenyl)ethanol | HCID 28894 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(2-hydroxy-2-phenylethyl)-3,5-dimethoxybenzamide | HCID 21998722 | 94.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06228868B1 |
|---|
| Source dataset | uspto-grants-2001_05 |
|---|
| ORD ID | ord-36ba17b6e39a493ba227457f28b989b9 |
|---|
| Source note | uspto-grants-2001_05 |
|---|