Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Tert-Butyl isocyanide | HCID 23577 | — |
| Reactant | HCID 178507418 | HCID 178507418 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178446833 | HCID 178446833 | 97.1% |
Reaction Steps
A mixture of 2.3 gm of 4-(p-aminophenyl)-1-H-imidazole, 1.25 gm of t-butylisonitrile, 0.2 gm of AgCl, and 0.11 gm of imidazole was heated at 100° C. for 13 hours. The thick reaction mixture was treated with 10% HCl and ethyl acetate. The acid solution was adjusted to pH 6.5 with 10% NaOH, treated with charcoal, filtered, and adjusted to an alkaline pH. The layer which separated was extracted with ethyl acetate. After drying, the organic solution was evaporated to dryness to yield 0.38 gm of the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04465841 |
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| Source dataset | uspto-grants-1984_08 |
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| ORD ID | ord-edef0fb393f741b0a457f8f86d72337d |
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| Source note | uspto-grants-1984_08 |
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