HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Diethyl 2-benzyloxymethyl-2-cyclohexylmalonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Benzyl chloromethyl ether | HCID 137983 | — |
| Reactant | Diethyl 2-cyclohexylmalonate | HCID 240541 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Diethyl 2-benzyloxymethyl-2-cyclohexylmalonate | HCID 19373401 | 107.2% |
Reaction Steps
Diethyl cyclohexylmalonate (18.7 g.) was added to a stirred suspension of sodium hydride (4.8 g. 50% dispersion in oil) in dry tetrahydrofuran (50 ml) under nitrogen. The mixture was refluxed, with stirring, for one hour. The mixture was cooled and benzyl chloromethyl ether (13.9 g.) in dry tetrahydrafuran (50 ml) was added and the mixture was refluxed, with stirring, for three hours. The mixture was cooled and poured into water. The aqueous mixture was extracted with ether. The ether extracts were washed with water, dried over anhydrous magnesium sulphate and evaporated in vacuo. Diethyl 2-benzyloxymethyl-2-cyclohexyl-malonate (30 g.) was obtained as a brown oil and was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04985582 |
| Source dataset | uspto-grants-1991_01 |
| ORD ID | ord-abf9346e37fc447f97e0e69f718acea6 |
| Source note | uspto-grants-1991_01 |