HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 5-Bromo-3-nitrothiophene-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl 5-bromo-3-nitrothiophene-2-carboxylate | HCID 57618723 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | 5-Bromo-3-nitrothiophene-2-carboxylic acid | HCID 29945545 | — |
Reaction Steps
1N sodium hydroxide solution (4 mL) was added to a solution of 5-bromo-3-nitrothiophene-2-carboxylic acid methyl ester (975 mg) in 1:1 THF/methanol (4 mL) and the solution was stirred at room temperature for 1 h. The solution was partitioned between water and ethyl acetate. The aqueous phase was brought to pH 1 with 2N HCl, extracted with ethyl acetate, dried over magnesium sulfate and concentrated. The product with the molecular weight of 252.04 (C5H2BrNO4S) was obtained in this way; MS (ESI): 252 and 254 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08853208B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-a5173de61bd34eaa81107fe602adecec |
| Source note | uspto-grants-2014_10 |