HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitric Acid → 2-Carboxy-3-methyl-5-nitrothiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | 3-Methyl-2-thenoic acid | HCID 90269 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 2-Carboxy-3-methyl-5-nitrothiophene | HCID 18376957 | 53% |
Reaction Steps
To a solution of 2-carboxy-3-methylthiophene (10 g, 70.3 mmol) in 80 mL of trifluoroacetic acid at 0° C. was added HNO3 (1.2 mL,1.0 eq.) dropwise. The reaction mixture was warmed to ambient temperature and after 4 hours another 1.0 eq. of HNO3 was added. The reaction mixture was made basic with aqueous sodium bicarbonate and washed with ethyl acetate. The aqueous layer was acidified with concentrated HCl and extracted with ethyl acetate. The organic layer was dried over sodium sulfate and concentrated in vacuo to afford 5.75 g (53%) of 2-carboxy-3-methyl-5-nitrothiophene and 2-carboxy-3-methyl-4-nitrothiophene, as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06380221B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-dc737adc7dc448e598b6371f8d8d050a |
| Source note | uspto-grants-2002_04 |