HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → Propenylamine, N-isobutylidene-2-methyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Isobutyraldehyde | HCID 6561 | — |
| Product | Propenylamine, N-isobutylidene-2-methyl- | HCID 220593 | — |
Reaction Steps
When isobutyraldehyde was reacted under conditions similar as described in Example I, above, for the preparation of dihydrothiazoles from ketones, no incorporation of sulfur occurred. However with a variation in the reaction, secondary aldehydes could be made to yield dihydrothiazoles in excellent yield. The reaction of isobutyraldehyde with ammonia yielded, via an intermediate, 2,6-dimethyl-4-azahepta-2,4-diene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05197545 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-da57cf17ce604ce5919124a547b9946f |
| Source note | uspto-grants-1993_03 |