HuagongsheHuagongshe Chemistry Print Report · For research reference only
ethyl N-(4-p-nitrophenyl-2-thiazolyl)carbamate → ethyl N-(4-p-aminophenyl-2-thiazolyl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | ethyl N-(4-p-nitrophenyl-2-thiazolyl)carbamate | HCID 5108134 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | ethyl N-(4-p-aminophenyl-2-thiazolyl)carbamate | HCID 15916633 | 72.4% |
Reaction Steps
In 500 ml of ethyl acetate, was dissolved 4 g of ethyl N-(4-p-nitrophenyl-2-thiazolyl)carbamate, followed by an addition of 3 g of a 10% palladium/carbon catalyst. The mixture was then subjected under normal pressure to reduction with hydrogen gas. The catalyst was filtered off. The filtrate was concentrated and subjected to column chromatography on silica gel. The reaction product was eluted with a chloroform/ethylacetate mixed solvent. The resulting product was then recrystallized from methanol to obtain 2.6 g of ethyl N-(4-p-aminophenyl-2-thiazolyl)carbamate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04511574 |
| Source dataset | uspto-grants-1985_04 |
| ORD ID | ord-a8636db37ef64995bc39fcef3690ec6f |
| Source note | uspto-grants-1985_04 |