HuagongsheHuagongshe Chemistry Print Report · For research reference only
Catechol → 4-Nitrocatechol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Catechol | HCID 289 | — |
| Reactant | o-Phenylene dibenzoate | HCID 69514 | — |
| Reactant | 4-Nitropyrocatechol dibenzoate | HCID 21425185 | — |
| Product | 4-Nitrocatechol | HCID 3505109 | 50% |
Reaction Steps
Further, the 3,4-dialkoxyanilines of formula I are obtained according to the invention in a yield of about 70% or more of the theoretical amount calculated on pyrocatechol whereas according to a known method comprising dibenzoylation of pyrocatechol, nitration of the pyrocatechol dibenzoate, hydrolysis 4-nitropyrocatechol dibenzoate, successive introduction of alkyl groups R1 and R2 into 4-nitropyrocatechol and reduction of 3,4-dialkoxy-nitrobenzene the 3,4dialkoxyanilines of formula I are obtained in a yield of less than 50% of the theoretical amount calculated on pyrocatechol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04035423 |
| Source dataset | uspto-grants-1977_07 |
| ORD ID | ord-b15851a34739407f8d29910316699482 |
| Source note | uspto-grants-1977_07 |