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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-Octyne, 8-chloro- | HCID 90360 | — |
| Reactant | 1-Bromo-2,6-dimethylundeca-2,5-diene | HCID 54263180 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Chloro-10,14-dimethylnonadeca-10,13-dien-7-yne | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03953499 |
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| Source dataset | uspto-grants-1976_04 |
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| ORD ID | ord-0cca801f0c7d4f3499e42b514095badf |
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| Source note | uspto-grants-1976_04 |
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