HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597684Generated: October 30, 2026
N,N-Dimethylaniline → 2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrile
https://huagongshe.com/reaction/597684
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | Diphosgene | HCID 10426 | — |
| Reactant | 2-(Hydroxyimino)-2-phenylacetonitrile | HCID 69998 | — |
| Reactant | 2-Chlorocarbonyloxyimino-2-phenylacetonitrile | HCID 53654775 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrile | HCID 93865 | — |
Reaction Steps
A solution of 2-hydroxyimino-2-phenylacetonitrile (14.6 g.) and dimethylaniline (13.2 g.) in a mixture of acetone (5 ml.) and benzene (80 ml.) was added to a solution of trichloromethyl chloroformate (phosgene dimer) (6.7 ml.) in benzene (30 ml.) under ice-cooling. The mixture was stirred for 6 hours at the same temperature and allowed to stand overnight. A mixture of tert-butyl alcohol (11.1 g.), pyridine (16.0 ml.) and benzene (20 ml.) was added dropwise, under ice-cooling, to the resultant mixture containing 2-chlorocarbonyloxyimino- 2-phenyl-acetonitrile. The mixture was stirred for 7 hours at room temperature and allowed to stand overnight. The reaction mixture was treated as described in the above Examples 2(A) to 2(F) to give 2-tert-butoxycarbonyloxyimino-2-phenylacetonitrile (17.0 g.), mp 84° to 86° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04014915 |
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| Source dataset | uspto-grants-1977_03 |
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| ORD ID | ord-80213ed12c7745878aa2c403264237ff |
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| Source note | uspto-grants-1977_03 |
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