HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia acetate → 3,3,5-Trimethylcyclohexanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia acetate | HCID 12432 | — |
| Reactant | 3,3,5-Trimethylcyclohexanone | HCID 13398 | — |
| Reactant | 1-Aminocyclohexyl hydroperoxide | HCID 19380058 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Cyclohexanone | HCID 7967 | — |
| Product | 3,3,5-Trimethylcyclohexanone | HCID 13398 | 64.3% |
Reaction Steps
1-Aminocyclohexyl hydroperoxide (13.1 g.), dihydroisophorone (14 g.), methanol (25 cc.) and ammonia acetate (1.0 g.) were mixed, stored at 0°C overnight and worked up as in the previous Example. Distillation gave cyclohexanone and dihydroisophorone (9.0 g.), an intermediate fraction (3.2 g.), b.p. below 100°C/0.7 mm., Hg., a fraction (8.1 g.), b.p. 110° - 114° 10.7 mm. of 3,3,5'-trimethyl-1,1'-peroxy-dicyclohexylamine (peroxide equivalent, 234; perchloric acid equivalent, 245; and residue (1.5 g.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03947406 |
| Source dataset | uspto-grants-1976_03 |
| ORD ID | ord-e8663b9339e748698fc7f0e0479767fa |
| Source note | uspto-grants-1976_03 |