HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082988Generated: November 2, 2026
N,N-Dimethylaniline → 2-(4-Methoxybenzyloxycarbonyloxyimino)-2-phenylacetonitrile
https://huagongshe.com/reaction/2082988
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | 4-Methoxybenzyl alcohol | HCID 7738 | — |
| Reactant | 2-(Hydroxyimino)-2-phenylacetonitrile | HCID 69998 | — |
| Reactant | 2-Chlorocarbonyloxyimino-2-phenylacetonitrile | HCID 53654775 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2-(4-Methoxybenzyloxycarbonyloxyimino)-2-phenylacetonitrile | HCID 3916227 | — |
Reaction Steps
A solution of dimethylaniline (6.0 ml.) in benzene (15 ml.) was added dropwise to a suspension of 2-hydroxyimino-2-phenylacetonitrile (7.3 g.) and phosgene (5.0 g.) in benzene (50 ml.) for 40 minutes under ice-cooling. The mixture was stirred for 2 hours at the same temperature and allowed to stand overnight. A solution of 4-methoxybenzyl alcohol (6.9 g.) and pyridine (4.0 ml.) in benzene (20 ml.) was added dropwise, for 30 minutes under ice-cooling, to the mixture containing 2-chlorocarbonyloxyimino-2-phenyl-acetonitrile. The mixture was stirred for 7 hours at room temperature. The reaction mixture was then washed with water, 1N hydrochloric acid, water, a sodium bicarbonate aqueous solution and water, and dried over magnesium sulfate. The solution was concentrated and the residual crystals were triturated in n-hexane and collected by filtration. The crystals were recrystallized from a mixture of ethyl acetate and n-hexane to give 2-(4-methoxybenzyl)oxycarbonyloxyimino-2-phenylacetonitrile (3.1 g.). Mp 112° to 113° C. The mother liquor was concentrated to give the desired compound (2.4 g.). Total yield (5.5 g.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04083848 |
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| Source dataset | uspto-grants-1978_04 |
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| ORD ID | ord-7b6ff00c8f894685a83cc7804dc908eb |
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| Source note | uspto-grants-1978_04 |
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