HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329257Generated: October 31, 2026
1,5-Dibromopentane → HCID 54472139, compound
https://huagongshe.com/reaction/329257
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,5-Dibromopentane | HCID 8100 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Potassium hydride | HCID 82127 | — |
| Reactant | HCID 12426219 | HCID 12426219 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 54472139 | HCID 54472139 | 59% |
Reaction Steps
Potassium hydride (995 mg) was suspended in 15 ml. of dioxane, and with ice cooling, 1.804 g of formaldehyde diisopropyl mercaptal S-oxide was added gradually. The mixture was stirred for 1 hour with ice cooling, and then 2.411 g of 1,5-dibromopentane was added. Then, the mixture was stirred for 18 hours at room temperature. Methylene chloride (100ml) was added, and the isoluble matter was separated by filtration. After the evaporation of the filtrate at reduced pressure, the residue was separated by column chromatography (basic alumina, eluted with benzene, methylene chloride, and ethyl acetate) to afford 1.463 g of cyclohexanone diisopropyl mercaptal S-oxide as a colorless oil. The yield was 59%. The physical properties and the results of elemental analysis were as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04020171 |
|---|
| Source dataset | uspto-grants-1977_04 |
|---|
| ORD ID | ord-ac3f66267eb94e6b8dd673b63e31d3f2 |
|---|
| Source note | uspto-grants-1977_04 |
|---|