HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1884598Generated: October 31, 2026
Ammonium formate → 4-tert-Butyl-2,6-diaminoanisole
https://huagongshe.com/reaction/1884598
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | 4-tert-Butyl-2,6-dinitroanisole | HCID 4252602 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-tert-Butyl-2,6-diaminoanisole | HCID 4177235 | 90% |
Reaction Steps
5-tert-Butyl-2-methoxy-1,3-dinitrobenzene (see Example 1, 1.9 g, 0.0075 mol) was added to EtOH (40 mL) under nitrogen purge. To this mixture, ammonium formate (4.9 g, 0.075 mol) was added in a single portion, followed by 10% palladium on carbon (0.75 g, 10 mole %), also in a single portion. This resulted in an immediate exotherm (temperature climbs to 30° C.), along with outgassing. Once the bubbling subsided, the mixture was slowly brought to reflux and maintained at this temperature for 3 h. An aliquot taken at this point showed over 93% conversion to a new, polar material. The mixture was filtered hot through a pad of diatomaceous earth, which was then washed twice with hot EtOH. The filtrate was concentrated under reduce pressure to obtain the title compound as a light grey solid (1.3 g, 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06765009B2 |
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| Source dataset | uspto-grants-2004_07 |
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| ORD ID | ord-ff6e978c9b03464eb9e43d5182e3c8fb |
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| Source note | uspto-grants-2004_07 |
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