HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → HCID 53687623, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | 1,3-Butadiene | HCID 7845 | — |
| Reactant | Allylamine | HCID 7853 | — |
| Reactant | HCID 54364347 | HCID 54364347 | — |
| Product | HCID 53687623 | HCID 53687623 | 80.5% |
Reaction Steps
The procedure described in Example 2 is repeated except that 110 g (1.13 mols) of N-isopropylidene-propenylamine [prepared by reacting acetone with allylamine, cf. B. A. Kazanskii et al., Zhurnal Organicheskoi Khimii, Volume 6, No. 11, 2197-9 (1970)] and 108 g (2 mols) of 1,3-butadiene are used. Distillation yields 187.0 g (0.91 mol) of 3,12,12-trimethyl-1-aza-1,5,9-cyclododecatriene; yield 80.5% of theory, based on converted N-isopropylidene-propenylamine (conversion 100%); boiling point 55° C./0.03 mm Hg; nD20 =1.4895.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04213901 |
| Source dataset | uspto-grants-1980_07 |
| ORD ID | ord-5e5992742cbb44b9bf19eafbb5571927 |
| Source note | uspto-grants-1980_07 |