HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 22925747, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | 1-Bromo-4-propylbenzene | HCID 136374 | — |
| Reactant | 1-Ethynyl-4-propylbenzene | HCID 2775133 | — |
| Reactant | HCID 22345880 | HCID 22345880 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 22925747 | HCID 22925747 | — |
Reaction Steps
The reaction was carried out in the same manner as in the step (i), except for using 4-n-propylphenylacetylene synthesized in the step (ii) and 1-(tert-butoxycarbonyloxy)-4-bromobenzene synthesized in the Example 4 instead of 1-n-propyl-4-bromobenzene and trimethylsilylacetylene, respectively. After completion of the reaction, the reaction solution was poured into an iced water, and the resultant solution was acidified by adding hydrochloric acid. After the resultant solid was collected by filtration, the collected solid was washed with water, dried, and recrystallized successively from hexane and ethanol to provide 4.1 g (12.1 mmol) of 1-[4-(tert-butoxycarbonyloxy)phenyl]-2-(4-n-propylphenyl)acetylene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07534547B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-7c7d30d5d4d34fc094fd51e2321991ca |
| Source note | uspto-grants-2009_05 |