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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
Reactant(4-Octylphenyl)acetaldehydeHCID 53716894—
ReactantButyllithiumHCID 178418339—
CatalystZincHCID 23994—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product1-Octyl-4-(prop-2-YN-1-YL)benzeneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04405810
Source datasetuspto-grants-1983_09
ORD IDord-b1dcac1cb3234f2496aece6f12c3f42f
Source noteuspto-grants-1983_09