HuagongsheHuagongshe Chemistry Print Report · For research reference only
Epichlorohydrin → HCID 23113189, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | [3-(Hydroxymethyl)-1-adamantyl]methanol | HCID 703011 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 23113189 | HCID 23113189 | — |
Reaction Steps
300 ml of dehydrated tetrahydrofuran containing 19.6 g (0.1 mol) of 1,3-bis(hydroxymethyl)adamantane and 5.3 g (0.22 mol) of sodium hydride was stirred in a nitrogen atmosphere at the reflux temperature for 2 hours. Thereto was dropwise added 20.4 g (0.22 mol) of epichlorohydrin, followed by stirring at the reflux temperature for 12 hours. To the reaction mixture was added 200 ml of chloroform, followed by washing with water. The chloroform layer was dried with magnesium sulfate. The dried chloroform layer was subjected to distillation under reduced pressure for solvent removal, whereby was obtained a white solid and oily matter.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07754903B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-5772540f082e4804b2a7718f9593e7bf |
| Source note | uspto-grants-2010_07 |