Ammonia → Pyridine

HRID 616245Notes

Reaction equation

HRID 616245 reaction equation
[CH2:1]=[CH:2][CH:3]=[CH2:4].C=O.N.F.F.F[Si](F)(F)F.[N:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>>[CH3:1][C:2]1[CH:16]=[N:15][CH:20]=[CH:4][CH:3]=1.[N:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1

Participants

7

Conditions

Temperature
320 °C

Procedure

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.

Sources & evidence

ORD record
ord-b3ed49ea32944ef1b9dbff8d801baf47
Source dataset
uspto-grants-1978_02
Patent number
US04073787

Reaction notes

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