HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylhydrazine → 4-[1-(t-Butylazo)cyclohexyl]-2-methylsemicarbazide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylhydrazine | HCID 6061 | — |
| Reactant | Isocyanate | HCID 105034 | — |
| Reactant | 1-t-Butylazo-1-isocyanatocyclohexane | HCID 21431172 | — |
| Solvent | Pentane | HCID 8003 | — |
| Product | 4-[1-(t-Butylazo)cyclohexyl]-2-methylsemicarbazide | HCID 21431146 | — |
Reaction Conditions
| Temperature | 5 °C |
|---|
Reaction Steps
To 8.2 grams (0.0392 moles) of 1-t-butylazo-1-isocyanatocyclohexane stirred with a magnetic stirrer in a 50 ml erlenmeyer flask and cooled to 5° C. was added 1.82 grams (0.0392 moles) of methylhydrazine. The reaction was very rapid and exothermic and became quite viscous. The reaction mixture was diluted with pentane and stirred for an additional 60 minutes at room temperature. The pentane was evaporated under reduced pressure leaving 9.0 grams (90% crude yield) of a yellow solid. The product melted at 169°-171° C. with decomposition. The infrared spectrum of the product contained a strong carbonyl band at 1660 cm-1 and a moderate NH band at 3320 cm-1. The isocyanate band at 2225 cm-1 was absent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04028344 |
| Source dataset | uspto-grants-1977_06 |
| ORD ID | ord-8d416c253721430bb3e24f8c083b70fb |
| Source note | uspto-grants-1977_06 |