HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfate → Cyclododecane, (2-methoxyethoxy)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium amide | HCID 24533 | — |
| Reactant | 2-cyclododecyloxyethanol | HCID 36121 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | Cyclododecane, (2-methoxyethoxy)- | HCID 174103 | — |
Reaction Steps
25 g of sodium amide was introduced into 150 ml of xylene and heated to boiling under agitation. Within one hour, 114 g (0.5 mol) of 2-hydroxyethyl-cyclododecyl-ether, dissolved in 750 ml of xylene, was allowed to drip into the boiling suspension. To complete the alcoholate formation, the mixture was heated under reflux for another two hours. Thereafter 44 g (0.35 mol) of dimethyl sulfate was added dropwise and the reaction mixture heated under reflux for another four hours. Then, the reaction mixture was poured into a mixture of ice and 35 g of sodium hydroxide. The organic phase was washed with water, dried over Na2SO4, and then fractionated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04317942 |
| Source dataset | uspto-grants-1982_03 |
| ORD ID | ord-b69bdbfd23cd42ecaf9a241fd5a20f98 |
| Source note | uspto-grants-1982_03 |