HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 13741088, compound → 4-tert-Butyltoluene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 13741088 | HCID 13741088 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-tert-Butyltoluene | HCID 7390 | — |
| Product | Isobutylene | HCID 8255 | — |
Reaction Steps
The diamine, 2,6-diamino-4-t-butyltoluene, was prepared from toluene. Alkylation of toluene with isobutene gave p-t-butyltoluene which was then nitrated to give 2,6-dinitro-4-t-butyltoluene. Reduction of the dinitro compound produced the diamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04963648 |
| Source dataset | uspto-grants-1990_10 |
| ORD ID | ord-35f3c19fb3224424ae13bd1c39c6b071 |
| Source note | uspto-grants-1990_10 |