HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methyl-3-p-tolyltriazine → 3-Methyl-6-tetradecyloxy-benzofuran-2-carboxylic acid, methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methyl-3-p-tolyltriazine | HCID 20261853 | — |
| Reactant | 3-Methyl-6-tetradecyloxybenzofuran-2-carboxylic acid | HCID 23335564 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3-Methyl-6-tetradecyloxy-benzofuran-2-carboxylic acid, methyl ester | HCID 86737277 | — |
Reaction Steps
0.4 g (1.03 mmoles) of 3-methyl-6-tetradecyloxy-benzofuran-2-carboxylic acid and 0.3 g (2.00 mmoles) of 1-methyl-3-p-tolyltriazine are stirred in ether and refluxed for 15 minutes. The mixture is then allowed to stand at room temperature for 1 hour. It is then refluxed for 15 minutes. The reaction mixture is worked-up by extraction with diethyl ether and HCl. The ether is distilled off and is replaced by dioxane. The resultant mixture is heated on a steam bath for 1 hour. It is then extracted with diethyl ether/HCl, H2O and NaHCO3 (aq.). The extract is evaporated and the ether replaced with methanol. The methyl ester of 3-methyl-6-tetradecyloxy-benzofuran-2-carboxylic acid is allowed to crystallize from the mixture.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04229467 |
| Source dataset | uspto-grants-1980_10 |
| ORD ID | ord-5dc7e5a6466641e5a1a015b7266fe95d |
| Source note | uspto-grants-1980_10 |