HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 14155738, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Aminobutyric acid methyl ester hydrochloride | HCID 2756383 | — |
| Reactant | HCID 11116082 | HCID 11116082 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 14155738 | HCID 14155738 | 26.1% |
Reaction Steps
Under nitrogen, 5.89 g (0.046 mole) of 3,3-dimethylglutaraldehyde, 7.03 g (0.0457 mole) of methyl 4-aminobutanoate hydrochloride (the compound of Example 9a), and 9 g of 5A molecular sieves were combined in 425 ml of chloroform at room temperature. 7.0 ml (0.05 mole) of triethylamine were added to the reaction mixture before it was warmed to reflux. After 21 hours the reaction mixture was cooled to room temperature, filtered, and the filtrate evaporated in vacuo. The residue was suspended in about 300 ml of ethyl ether and filtered. The filtrate was evaporated in vacuo to yield 8.56 g of crude product. The crude product was distilled to yield 2.5 g of the title compound as a clear liquid, bp 95° C./0.2 mm Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04742068 |
| Source dataset | uspto-grants-1988_05 |
| ORD ID | ord-3392d5cb897f4c1a950e3fed2eb4240c |
| Source note | uspto-grants-1988_05 |