HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-Chloro-5-hydroxy-5-methyl-6-heptyne
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 6-Chlorohexan-2-one | HCID 82468 | — |
| Reactant | HCID 178462446 | HCID 178462446 | — |
| Product | 1-Chloro-5-hydroxy-5-methyl-6-heptyne | HCID 13198054 | — |
Reaction Steps
200 g (2.17 mol) of lithium acetylide in the form of the ethylenediamine complex were suspended in 800 ml of dry dioxane and, while stirring vigorously and cooling in ice, 269.2 g (2.0 mol) of 1-chloro-5-hexanone were rapidly added dropwise, during which the temperature rose to 48° C. The exothermic reaction was allowed to subside while stirring for 3 hours without further external cooling, 500 ml of water were cautiously added, the mixture was filtered, most of the dioxane was distilled off under reduced pressure, the aqueous phase was extracted exhaustively with chloroform, the extract was dried over sodium sulfate, the solvent was evaporated off under reduced pressure, and the residue was subjected to fractional distillation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05965555 |
| Source dataset | uspto-grants-1999_10 |
| ORD ID | ord-645b846b761c4cf7a9c407285bf7c9ca |
| Source note | uspto-grants-1999_10 |