HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propargyl bromide → 2-Propargyloxy-2-phenyl-3-butyne
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propargyl bromide | HCID 7842 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-Hydroxy-3-phenyl-1-butyne | HCID 92098 | — |
| Reactant | Tetrabutyl ammonium hydrogen sulfate water | HCID 86750630 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2-Propargyloxy-2-phenyl-3-butyne | HCID 11252392 | 65% |
Reaction Steps
Propargyl bromide (22 g, 0.15 mol) was dissolved in 140 ml of n-hexane. This solution, 2-phenyl-3-butyne-2-ol (14.6 g, 0.1 mol), NaOH (60 g, 1.5 mol) and a catalytic amount of tetrabutyl ammonium hydrogen sulfate/water (120 ml) were mixed, reacted for 24 hours at an ambient temperature and refluxed for 30 minutes. After completion of the reaction, the mixture was cooled to an ambient temperature and water (100 ml) was added. The organic phase was extracted with 30 ml of n-hexane, three times. The extracted organic solvent was dried with anhydrous magnesium sulfate, filtered and evaporated to separate. b.p.: 61° C./0.5 mmHg; yield: 65%; MS: m/e 184 (parent), 129 (base).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05616669 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-0eda761b3ecf455a8a5934f3ae9aab88 |
| Source note | uspto-grants-1997_04 |