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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606681Generated: November 3, 2026

Ammonium Chloride → 1-Chloro-10,14-dimethylnonadeca-10,13-dien-7-yne

https://huagongshe.com/reaction/1606681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Octyne, 8-chloro-HCID 90360—
Reactant1-Bromo-2,6-dimethylundeca-2,5-dieneHCID 54263180—
ReactantHCID 178418443HCID 178418443—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product1-Chloro-10,14-dimethylnonadeca-10,13-dien-7-yneHCID 53671320—

Reaction Steps

A solution of 12.0 g. of 1-chlorooct-7-yne in 20 ml. of tetrahydrofuran is added to a mixture of 27 ml. of 3N ethyl magnesium bromide in ether and 50 ml. of tetrahydrofuran. The mixture is stirred and heated under reflux for 30 min. under nitrogen, then 0.45 g. of powdered cuprous chloride is added and heating and stirring is continued for 20 min. A solution of 20.0 g. of 1-bromo-2,6-dimethyl-2,5-undecadiene in 15-ml. of tetrahydrofuran is added and the mixture is heated under reflux for 10 hrs., then allowed to stand for about 18 hrs., and poured into saturated aqueous ammonium chloride and ether. The mixture is filtered and the ether solution is separated, washed with water, dried over sodium sulfate, and evaporated to leave a residue comprising 1-chloro-10,14-dimethylnonadeca-10,13-dien-7-yne.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03953499
Source datasetuspto-grants-1976_04
ORD IDord-0cca801f0c7d4f3499e42b514095badf
Source noteuspto-grants-1976_04