HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 74083Generated: October 25, 2026
Potassium Formate → Ethyl 2-(4-aminophenyl)-2-methylpropanoate
https://huagongshe.com/reaction/74083
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Formate | HCID 2735122 | — |
| Reactant | Ethyl 2-methyl-2-(4-nitrophenyl)propanoate | HCID 15544079 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 2-(4-aminophenyl)-2-methylpropanoate | HCID 15544083 | 85.1% |
Reaction Steps
A solution of ethyl 2-(4-nitrophenyl)-2-methylpropanoate (900 mg, 3.8 mmol) in EtOH (10 mL) was treated with 10% Pd—C (80 mg) and heated to 45° C. A solution of potassium formate (4.10 g, 48.8 mmol) in H2O (11 mL) was added over a period of 15 min. The reaction mixture was stirred at 65° C. for 2 h and then treated with additional 300 mg of Pd/C. The reaction was stirred for 1.5 h and then filtered through Celite. The solvent volume was reduced by approximately 50% under reduced pressure and extracted with EtOAc. The organic layers were dried over Na2SO4 and the solvent was removed under reduced pressure to yield ethyl 2-(4-aminophenyl)-2-methylpropanoate (G-1) (670 mg, 85%). 1H NMR (400 MHz, CDCl3) δ 7.14 (d, J=8.5 Hz, 2H), 6.65 (d, J=8.6 Hz, 2H), 4.10 (q, J=7.1 Hz, 2H), 1.53 (s, 6H), 1.18 (t, J=7.1 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08829204B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-0fb9aa8c8393480bb565697a4165ab56 |
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| Source note | uspto-grants-2014_09 |
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