Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl chloride | HCID 7850 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 53943258 | HCID 53943258 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 54210645 | HCID 54210645 | 35.9% |
Reaction Steps
Into a 250 ml 4-neck flask equipped with stirrer, reflux cooler and dropping funnel, 20 g (0.5 moles) of solid sodium hydroxide, 80 ml of toluene and 5 g of tetrabutylammonium bromide are first introduced and heated to 80° C. To this 2-phase system, a mixture of 50 g (0.41 moles) of 2-propyl-2-pentenenitrile and 31.4 g (0.41 moles) of allyl chloride were added in doses within 30 minutes. The reaction mixture was maintained for 2 more hours at a temperature of 75° C. Further work proceeded as in Example 1. A yield of 24 g of desired product, corresponding to 29.4% of the theoretical, was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04625046 |
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| Source dataset | uspto-grants-1986_11 |
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| ORD ID | ord-a697c163825d4c26a8852fe8b5846697 |
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| Source note | uspto-grants-1986_11 |
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