Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrite | HCID 946 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2-Propylvaleronitrile | HCID 83330 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Product | Valpromide | HCID 71113 | — |
Reaction Steps
As regards the hydrolysis of the di-n-propyl acetonitrile, this will advantageously be carried out by means of 80% by weight sulphuric acid in the proportion of 3 to 5 g of dilute acid/g of nitrile, for example, 3.75 g of dilute acid/g of nitrile over a period of 90 minutes at 80°-85° C. and adding to the resulting amide an aqueous solution of sodium nitrite in the proportion of 1.4 mol of nitrite/mol of di-n-propyl acetonitrile, the reaction taking place for 2 hours at 40°-50° C. It will also be just as advantageous to use a 75% by weight sulphuric acid aqueous solution in the proportion of 1.7 g of dilute acid/g of nitrile for 30 minutes at 140° C., to obtain the intermediate di-n-propyl acetamide, which is hydrolysed in the same sulphuric acid medium in the presence of sodium nitrite in the proportion of 1.4 to 1.5 mol of nitrite/mol of di-n-propyl acetonitrile for one hour at 50°-60° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04127604 |
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| Source dataset | uspto-grants-1978_11 |
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| ORD ID | ord-c5898a57f50a472bbcac5877e42c97cc |
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| Source note | uspto-grants-1978_11 |
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