HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1,5-Di[1-(t-butylazo)-cyclohexylaminothiocarbonyl]carbohydrazide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Carbohydrazide | HCID 73948 | — |
| Reactant | 1-t-Butylazo-1-isothiocyanatocyclohexane | HCID 21431144 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1,5-Di[1-(t-butylazo)-cyclohexylaminothiocarbonyl]carbohydrazide | HCID 86734828 | — |
Reaction Steps
To a slurry of 2.25 grams (.025 moles) of carbohydrazide in 30 ml of methanol stirred by a magnetic stirrer in a 50 ml erlenmeyer flask was added 11.3 grams (.05 moles) of 1-t-butylazo-1-isothiocyanatocyclohexane (from Example I). The reaction was stirred overnight, during which time complete solution was obtained. The next morning the solution was poured into 200 ml water and the product extracted with methylene chloride. The methylene chloride extract was washed with water, dried over anhydrous Na2SO4, filtered and the methylene chloride evaporated under reduced pressure to leave 11.9 grams (87.5% crude yield) of a yellow viscous liquid that slowly crystallized.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04028344 |
| Source dataset | uspto-grants-1977_06 |
| ORD ID | ord-5335592bf88b4e8a94ff3c3b5073e960 |
| Source note | uspto-grants-1977_06 |