HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1995774Generated: October 27, 2026
Carbon tetrabromide → 1-Octyl-4-(prop-2-YN-1-YL)benzene
https://huagongshe.com/reaction/1995774
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | (4-Octylphenyl)acetaldehyde | HCID 53716894 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Octyl-4-(prop-2-YN-1-YL)benzene | HCID 20488001 | — |
Reaction Steps
p-(n-Octyl)phenylacetaldehyde (1 mmole, prepared as described in paragraph A of this example) is dissolved in methylene chloride, and treated with carbontetrabromide (4 mmole), triphenylphosphine (4 mmole) and zinc dust (4 mmole) at room temperature. The reaction mixture is then diluted with ethyl ether and filtered. The filtrate is washed with water, dried and evaporated to give an oily residue. This residue is dissolved in tetrahydrofuran and treated with n-butyl lithium (2.1 mmole) at -78° C. for one hour and then at room temperature until the reaction ceases. The reaction mixture is poured onto water, the pH adjusted to 7, and extracted with methylene chloride. The methylene chloride extract is washed with water, dried and the solvent removed by evaporation. Distillation under reduced pressure affords p-(n-octyl)benzylacetylene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04405810 |
|---|
| Source dataset | uspto-grants-1983_09 |
|---|
| ORD ID | ord-b1dcac1cb3234f2496aece6f12c3f42f |
|---|
| Source note | uspto-grants-1983_09 |
|---|