Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclohexyl isocyanate | HCID 18502 | — |
| Reactant | Isocyanate | HCID 105034 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | 1,4-Dioxane | HCID 31275 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Cyclohexylformamide | HCID 13017 | 83.5% |
Reaction Steps
A solution of cyclohexyl isocyanate (1.25 g.; 0.01 mole) in 100 ml. anhydrous 1,4-dioxane containing two drops of anhydrous triethylamine was mixed with 0.5 gram 10% Pd-on-carbon and shaken at a pressure of 50 p.s.i. of hydrogen on a Parr low pressure hydrogenator. The uptake of hydrogen was complete in two hours. Work up, as in Example 1, gave 1.15 g. of colorless oil containing a trace of isocyanate. The product was purified by slurrying the oil with Skellysolve B, chilling at -15° C. and decanting the supernatant from the crystalline formamide. After drying under high vacuum, the weight of title product was 1.06 g. (83.5% yield). The ir, nmr and glc were identical to an authentic sample.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04125724 |
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| Source dataset | uspto-grants-1978_11 |
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| ORD ID | ord-3525f5417a87431d84a4f5bdb0f30d16 |
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| Source note | uspto-grants-1978_11 |
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