Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 10081040 | HCID 10081040 | — |
| Reactant | HCID 14986661 | HCID 14986661 | — |
| Reactant | Methyl 5-methoxycarbonyl-oct-7-enoate | HCID 14986662 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-Carbomethoxy-oct-7-enenitrile | HCID 14986703 | — |
Reaction Steps
Methyl 1-allyl-2-oxocyclopentane-1-carboxylate (1.1 Kg) is added to 1,100 mL of methanol previously saturated with ammonia gas at ice bath temperature. The reaction mixture is stirred first at ice bath temperature and then at room temperature overnight with constant introduction of ammonia. The reaction mixture is evaporated to dryness to yield starting material and a mixture of 5-carbomethoxyoct-7-enoic acid amide and methyl 5-carbomethoxy-oct-7enoate. The residue is distilled under reduced pressure to yield a mixture of the diester and ester amide. A portion (25 g) is added dropwise over 40 minutes to 23.6 g of thionyl chloride and the mixture is heated at 80° for 30 minutes. The reaction mixture is evaporated to dryness under water vacuum and then distilled under high vacuum to yield 5-carbomethoxy-oct-7-enenitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05025025 |
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| Source dataset | uspto-grants-1991_06 |
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| ORD ID | ord-04d4bf0d781844c98d76519c4eba0fca |
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| Source note | uspto-grants-1991_06 |
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