HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744717Generated: November 1, 2026
Dimethyl Sulfoxide → 3-Decyloxymethylcyclohexene
https://huagongshe.com/reaction/1744717
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | 1-Decanol | HCID 8174 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 11459813 | HCID 11459813 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Decyloxymethylcyclohexene | HCID 22222976 | — |
Reaction Steps
A 500 mL round bottom flask equipped with a mechanical stirrer was charged with 23.7g (0.15 mol) decyl alcohol, and 150 mL of DMSO. Sodium hydride (4.22 g, 95% in purity; 0.167 mol) was slowly added to above mixture in an ice bath over 20 min. After the above mixture was reacted at room temperature for 3 hrs, the reaction mixture was cooled to room temperature. 3-Cyclohexene-1-methanol tosylate (39.9 g, 0.15 mol) was slowly added to the above mixture over 20 min. The reaction was carried at room temperature overnight, then 80° C. for 3 hrs. The reaction mixture was added to water (150 mL), and then extracted with chloroform (3×150 niL), washed to water (2×100 mL) and dried with sodium sulfate. The solvent was evaporated and the residue distilled to give pure product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07018559B2 |
|---|
| Source dataset | uspto-grants-2006_03 |
|---|
| ORD ID | ord-38c01c9fe730490bb9f82ef733d010fe |
|---|
| Source note | uspto-grants-2006_03 |
|---|