HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 4-Decyne, 1-bromo-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Lithium Bromide | HCID 82050 | — |
| Reactant | 1-Chloro-4-decyne | HCID 141322 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Decyne, 1-bromo- | HCID 22621683 | — |
Reaction Steps
1-Bromodec-4-yne was prepared from 1-chlorodec-4-yne. The 1-chlorodec-4-yne (10.6 g, 61 mmol) and 25 g of lithium bromide were refluxed in 80 ml of THF for 21 hours. The conversion was 74%. Ether was added, the reaction mixture was washed with water (2×) and brine, dried over magnesium sulfate and stripped. The product was dissolved in 70 ml of THF and refluxed for 8 hours with an additional 25 g of lithium bromide. This gave 95% conversion of the chloride to the bromide. The same workup provided 11.36 g of 1-bromodec-4-yne.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06365549B2 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-f6c0f997f4574b7d99e3a5984f3dc778 |
| Source note | uspto-grants-2002_04 |