Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Aldoxime | HCID 7863 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Chlorine | HCID 24526 | — |
| Reactant | Ethanimidoyl chloride, N-hydroxy- | HCID 69633 | — |
| Reactant | Methyl 2-methyl-3-mercaptopropionate | HCID 107231 | — |
| Solvent | Ammonium Hydroxide | HCID 14923 | — |
| Product | HCID 86254502 | HCID 86254502 | — |
Reaction Steps
Using the procedure described in Example I 33 grams (0.25 m) of methyl 3-mercapto-2-methylpropionate and 10 grams (0.25 m) of NaOH was caused to react with acetohydroximoyl chloride prepared from 15 g (0.25 m) of acetaldoxime and 18 g (0.25 m) of chlorine. After reaction the crude reaction product was placed in a pyrex pressure bottle to which was added 200 ml of concentrated ammonium hydroxide. The bottle was sealed and the mixture was stirred by means of a magnetic stirring bar for two days at ambient temperature. The bisphasic reaction mixture was then extracted with ether and the lower, aqueous phase was concentrated in vacuo to produce 3 g of a residue which crystallized on standing. An infrared spectrum supported the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04454134 |
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| Source dataset | uspto-grants-1984_06 |
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| ORD ID | ord-7e1fa94d8d8b441092eb0b806a946c78 |
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| Source note | uspto-grants-1984_06 |
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