HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Bromo-3-nitro-thiophene-2-carbaldehyde → 5-Bromo-3-nitrothiophene-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Bromo-3-nitro-thiophene-2-carbaldehyde | HCID 86247493 | — |
| Reactant | Jones' reagent | HCID 131709961 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Bromo-3-nitrothiophene-2-carboxylic acid | HCID 29945545 | 80% |
Reaction Steps
5Bromo-3-nitrothiophene-2-carbaldehyde (0.5953 g, 2.5012 mmol, prepared according to Sone, C; Matsuki, Y Bull Chem Soc Japan, 1963, 36(5), 618-20.) was dissolved in acetone (5 mL) and Jones Reagent (1.5 mL) was added. The reaction was stirred at RT for 1 h. The reaction was diluted with water (30 mL) and extracted with EtOAc (3×30 mL). The combined organics were washed With water (4×100 mL), dried over MgSO4 filtered and concentrated to give 0.4993 g (1.9892 mmol, 80%) of the product as a light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07285557B2 |
| Source dataset | uspto-grants-2007_10 |
| ORD ID | ord-3e7345aab5a9475e996762caf0632f32 |
| Source note | uspto-grants-2007_10 |