HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35963Generated: October 29, 2026
Nitric Acid → HCID 178475040, compound
https://huagongshe.com/reaction/35963
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 178475038 | HCID 178475038 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178475040 | HCID 178475040 | — |
Reaction Steps
28.3 ml (0.3 mol) acetic acid anhydride are mixed with 375 ml acetonitrile, cooled in an ice-bath to 0°-5° C. and 12.6 ml (0.3 mol) 100% nitric acid added dropwise. After 30 minutes, 15.7 g (0.1 mol) solid trans-N-acetyl-4-hydroxycyclohexylamine are added thereto with stirring and cooling at 0°-5° C. The reaction mixture is further stirred for 3 h at 0°-5° C. and subsequently allowed to flow carefully into a solution of 150 g (18 mol) sodium hydrogen carbonate in 500 ml ice water. After extraction with ethyl acetate, drying of the organic phase with sodium sulphate and distilling off in a vacuum, there remain 17.8 g of crude product. After recrystallisation from ethyl acetate, there are obtained 10.3 g of the title compound of the m.p. 146°-148° C., i.e. 50% of theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05411989 |
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| Source dataset | uspto-grants-1995_05 |
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| ORD ID | ord-5772ed044caa42808bd1e0d3d45fadff |
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| Source note | uspto-grants-1995_05 |
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