Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acrylonitrile | HCID 7855 | — |
| Reactant | Calcium Carbonate | HCID 10112 | — |
| Reactant | Chlorine | HCID 24526 | — |
| Reactant | 2,3-Dichloropropiononitrile | HCID 92935 | — |
| Product | Acrylonitrile | HCID 7855 | — |
| Product | 2-Chloroacrylonitrile | HCID 70198 | 4.2% |
| Product | 2,3-Dichloropropiononitrile | HCID 92935 | 90.5% |
Reaction Steps
In the same way as in Example 1, 53.1 g of acrylonitrile was chlorinated at 20° to 25° C. in the presence of 20.0 g (0.2 mole) of anhydrous calcium carbonate. When the weight of the reaction solution reached 124 g which was the weight showing that 2,3-dichloropropionitrile was formed in a calculated amount, the reaction was stopped. Chlorine dissolved in the reaction solution was removed with nitrogen. The weight of the reaction product at this time was 116.6 g. The catalyst was separated by filtration, and the reaction solution was distilled under reduced pressure to afford 0.7 g of acrylonitrile as a first fraction boiling at 23° C. (100 mmHg), 3.1 g (yield of 4.2% based on acrylonitrile) of 2-chloroacrylonitrile as a second fraction boiling at 43°-44° C. (150 mmHg), and 112.3 g (yield of 90.5% based on acrylonitrile) of 2,3-dichloropropionitrile as a third fraction boiling at 62°-63° C. (13 mmHg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04350643 |
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| Source dataset | uspto-grants-1982_09 |
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| ORD ID | ord-b3c0f83f714743168460633381c9e9fc |
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| Source note | uspto-grants-1982_09 |
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