HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 962376Generated: October 30, 2026
Isoamyl Nitrite → 2-hydroxyimino-2-(4-methoxyphenyl)acetonitrile
https://huagongshe.com/reaction/962376
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isoamyl Nitrite | HCID 8053 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Benzeneacetonitrile, 4-methoxy- | HCID 66031 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 2-hydroxyimino-2-(4-methoxyphenyl)acetonitrile | HCID 4398191 | 80.6% |
Reaction Steps
64.5 g of methanol, 365 g of xylene, 80 g of sodium hydroxyde (2 mol) and 147 g (1 mol) of 4-methoxyphenylacetonitrile are charged to a reactor. Then 125 g (1.07 mol) of isopentyl nitrite are added dropwise at 40° C. over 2 hours. The reaction mixture is stirred initially for 2 hours at this temperature and the n for 20 hours at room temperature. Afterwards the reaction mixture is diluted with water to form an emulsion and the pH is adjusted to 14 with aqueous sodium hydroxide and the organic phase is separated. The aqueous phase is acidified with hydrochloric acid and the product is extracted with ether. The ether phase is dried and the ether is stripped off. Recrystallisation from toluene gives 142 g of α-hydroxyimino-4-methoxy-benzylcyanide, corresponding to a yield of 80.6% of theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05759740 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-da25d505a29a43a4b3348da8f66e621b |
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| Source note | uspto-grants-1998_06 |
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