HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylamine → 2,4-Heptadiyn-1-ol, 6-methoxy-6-methyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | Propargyl alcohol | HCID 7859 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | 1-Butyne, 1-bromo-3-methoxy-3-methyl- | HCID 10352226 | — |
| Catalyst | Cuprous chloride | HCID 62652 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2,4-Heptadiyn-1-ol, 6-methoxy-6-methyl- | HCID 9989423 | 89.6% |
Reaction Steps
200 ml of a 70% aqueous solution of ethyamine, 1 g of copper(I) chloride, 5 g of hydroxylamine hydrochloride and 25 g of propargyl alcohol were dissolved in 500 ml of methanol, and with ice cooling and stirring, a methanol solution (100 ml) of 74 g of 1-bromo-3-methoxy-3-methyl-1-butyne was added. The mixture was stirred at room temperature for 1 hour, and then the solvent was evaporated. Water and ethyl acetate were added, and the insoluble material was removed by filtration. The organic layer separated was worked up in a customary manner, and the product was purified by vacuum distillation ( b.p. -97° C. / 2 mmHg ) to give 57 g of the captioned compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05306728 |
| Source dataset | uspto-grants-1994_04 |
| ORD ID | ord-1a16649ea5e848ea93612e0392f12700 |
| Source note | uspto-grants-1994_04 |