Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Isocyanate | HCID 105034 | — |
| Reactant | 1-t-Butylazo-1-isocyanatocyclohexane | HCID 21431172 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21431325 | HCID 21431325 | — |
Reaction Steps
To 50 ml of isopropanol in a 125 ml erlenmeyer flask stirred with a magnetic stirrer, was slowly added 2.1 grams (0.05 moles) of 57% sodium hydride. After the temperature came back to 25° C., 10.5 grams (0.05 moles) of 1-t-butylazo-1isocyanatocyclohexane was added dropwise over 5 minutes. After the addition was complete, the reaction was stirred an additional 30 minutes at room temperature. Gas chromatography indicated that the 1-t-butylazo-1-isocyanatocyclohexane had reacted almost immediately. The reaction mixture was poured into 300 ml water and the product extracted with 100 ml pentane. The pentane extract was separated, washed with water, 10% NaHCO3 solution, dried over anhydrous Na2SO4, filtered and the pentane evaporated under reduced pressure to leave 11.0 grams (81.5% crude yield) of a yellow liquid. The product had a strong carbonyl band at 1725 cm-1 and a sharp NH band at 3400 cm-1 in its infrared spectrum and the isocyanate band at 2225 cm-1 was absent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04028344 |
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| Source dataset | uspto-grants-1977_06 |
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| ORD ID | ord-c262462fdf5c4107b2260b5cf25fbbb7 |
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| Source note | uspto-grants-1977_06 |
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