HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 20244240, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 20244258 | HCID 20244258 | — |
| Reactant | HCID 86739684 | HCID 86739684 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 20244240 | HCID 20244240 | — |
Reaction Steps
A mixture of 24.9 g. (0.10 mole) 3-methoxy-5-(1,1-dimethylheptyl)aniline, 34.5 g. (0.12 mole) methyl dl-3,6-dibromocaproate, 15 g. triethylamine and 100 ml. ethyl ether is stirred under nitrogen at room temperature for 20 hours. The ether is evaporated and the residue heated at 90°-120° C. for three hours. Additional methyl dl-3,6-dibromocaproate (5 g.) and triethylamine (5 g.) is added and heating continued at 90° C. for 2 hours and finally at 120° C. for one hour. The reaction mixture is worked up as described in Example 16 to provide the methyl ester of the desired product which is hydrolyzed in methanolic sodium hydroxide by the method of Example 17 to provide the title acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04476131 |
| Source dataset | uspto-grants-1984_10 |
| ORD ID | ord-8e43205887064f3588d3aac42b6f0819 |
| Source note | uspto-grants-1984_10 |