HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Butanol → HCID 178450655, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Butanol | HCID 263 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Urea | HCID 1176 | — |
| Reactant | Methyl 4-Formylbenzoate | HCID 15294 | — |
| Reactant | 1,1,4,4-Tetramethyl-6-ethynyl-1,2,3,4-tetrahydronaphthalene | HCID 14726549 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 178450655 | HCID 178450655 | — |
Reaction Steps
21 g (0.1 mole) of 6-ethynyl-1,2,3,4-tetrahydro-1,1,4,4-tetramethylnaphthalene, 16 g (0.1 mole) of methyl 4-formylbenzoate, 9 g (0.15 mole) of urea and 15 ml of concentrated sulfuric acid in 50 ml of n-butanol were refluxed for 4 hours. After cooling, the mixture was poured onto 500 ml of water, 100 ml of ether were added and stirring was carried out for 5 minutes. A solid was precipitated between phases. In a shaking funnel, the washed with water and then shaken thoroughly with 200 ml of petroleum ether. The precipitate was filtered off under suction and washed with petroleum ether. 6.5 g of the title compound of melting point 267°-277° C. were obtained in this manner.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05196532 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-e78864ecd2a941718326c47503d2a814 |
| Source note | uspto-grants-1993_03 |