HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylamine → 4-Benzyloxy-1-dimethylaminocyclohexanecarbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Dimethylamine, hydrochloride | HCID 10473 | — |
| Reactant | 4-(Benzyloxy)cyclohexanone | HCID 10987369 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Benzyloxy-1-dimethylaminocyclohexanecarbonitrile | HCID 21093240 | — |
Reaction Steps
A mixture of 130 ml of 7.9 molar aqueous dimethylamine solution, 16 ml of methanol, 20.0 g of 4-benzyloxycyclohexanone, 23.2 g of dimethylamine hydrochloride and 15.3 g of potassium cyanide was stirred for 65 hours at room temperature; extraction was carried out four times using 120 ml of diethyl ether each time, and the combined extracts were concentrated; 100 ml of dichloromethane were added to the residue, the phases were separated, and the organic phases were dried over sodium sulfate, filtered and concentrated. 24.5 g of 4-benzyloxy-1-dimethylaminocyclohexanecarbonitrile were obtained in the form of a yellowish oil which slowly solidified.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07211694B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-4c61180a1d2c49dba50468e13509358b |
| Source note | uspto-grants-2007_05 |