HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429169Generated: October 30, 2026
Sodium Cyanide → 2-(Hydroxyimino)-3-methoxy-3-methylbutanenitrile
https://huagongshe.com/reaction/429169
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | Chlorine | HCID 24526 | — |
| Reactant | HCID 86181628 | HCID 86181628 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Methanol--water (1/1) | HCID 22242641 | — |
| Product | 2-(Hydroxyimino)-3-methoxy-3-methylbutanenitrile | HCID 71413883 | — |
Reaction Steps
53.6 g (0.46 mol) of 2-methoxy-2-methylpropionaldehyde oxime in ether (about 1 M) are initially taken at from −5 to −10° C. 35.8 g (0.5 mol) of chlorine gas are passed in, after which stirring is carried out for 1 hour at this temperature and the mixture is then evaporated down at 10° C. and the residue is taken up in diethyl ether. 24.7 g (0.5 mol) of sodium cyanide in 375 ml of 20:1 methanol/H2O are initially taken at 10° C. and the above ethereal solution is rapidly added dropwise. After 4 hours at room temperature, the mixture is filtered under suction and the residue is washed with twice 100 ml of methanol. The combined solutions are evaporated down and the residue is partitioned between methyl tert-butyl ether and water. Drying the organic phase over Na2SO4, evaporating down and crystallizing from dichloromethane-/n-hexane give 41.1 g (63% of theory) of a white powder of melting point 102-104° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06316459B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-63ca49c25f8d451fa741c668c123f044 |
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| Source note | uspto-grants-2001_11 |
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