HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2,6-DIMETHOXYBENZAMIDE
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,6-Dimethoxybenzoic Acid | HCID 15109 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,6-DIMETHOXYBENZAMIDE | HCID 89078 | 54% |
Reaction Steps
5.0 of 2,6-dimethoxybenzoic acid suspended in 200 ml of anhydrous methylene chloride are added with 7.65 ml of triethylamine and then with 3.6 ml of oxalyl chloride. The mixture after being stirred at room temperature for three hours is concentrated under reduced pressure, cooled with ice, added with 10 ml of concentrated ammonia, then stirred for half an hour, then again evaporated under reduced pressure, taken with water and filtered. The solid so obtained, after crystallization from methanol, gives 2,6-dimethoxybenzamide with melting point 208°-209° C.; yield is 54%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04888283 |
| Source dataset | uspto-grants-1989_12 |
| ORD ID | ord-aa8cc7d5d2714bc587a20da47d29524f |
| Source note | uspto-grants-1989_12 |