Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 1,3-Butadiene | HCID 7845 | — |
| Reactant | HCID 11137276 | HCID 11137276 | — |
| Product | Pyridine | HCID 1049 | 44% |
| Product | 3-Methylpyridine | HCID 7970 | — |
Reaction Steps
Following the same general procedure as in Example 1, a gaseous mixture of 1,3-butadiene (2.1% by volume), formaldehyde (1.7% by volume), ammonia (7.8% by volume), air 31.5% by volume), steam (33.2% by volume) and nitrogen (23.7% by volume) was passed through a fluidised bed of "Synclyst" catalyst (previously treated with fluosilicic acid in an amount corresponding to 5% by weight of the catalyst) maintained at 320° C. The contact time was 4.9 seconds and the mixture was passed over a period of 4 hours during which time 0.41 mole of 1,3-butadiene and 0.33 mole of formaldehyde were fed. 0.352 mole of unreacted butadiene was recovered corresponding to a molar conversion of 14.8%. A total of 0.027 mole of pyridine and 0.0055 mole of 3-methylpyridine were formed, corresponding to a pyridine yield of 44% of the butadiene consumed.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04073787 |
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| Source dataset | uspto-grants-1978_02 |
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| ORD ID | ord-b3ed49ea32944ef1b9dbff8d801baf47 |
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| Source note | uspto-grants-1978_02 |
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