HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexylamine → N-(1-adamantyl)-N'-cyclohexylthiourea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexylamine | HCID 7965 | — |
| Reactant | Adamantyl isothiocyanate | HCID 107279 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-(1-adamantyl)-N'-cyclohexylthiourea | HCID 4328819 | — |
Reaction Steps
The thiourea is prepared by reacting 19.3 g. (0.1 mole) of 1-adamantyl isothiocyanate with 10 g. (0.1 mole) of cyclohexylamine in 250 ml. of ether at room temperature for 3 hrs. The thiourea which separates from solution is collected: 23.5 g., mp. 175-175.5. Evaporation of the ether filtrate to a small volume gives a second crop, 5.2 g., mp. 176-178. The combined yield is 28.7 g. (98.5 percent). A sample is recrystallized from alcohol and melts at 176°-177°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04007181 |
| Source dataset | uspto-grants-1977_02 |
| ORD ID | ord-f19c9dab45e24f08988a03c2f86f46fd |
| Source note | uspto-grants-1977_02 |