HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 3-bromothiophene-2-carboxylate → 3-Bromothiophene-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 3-bromothiophene-2-carboxylate | HCID 2740074 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 3-Bromothiophene-2-carboxylic acid | HCID 2739688 | 97.3% |
Reaction Steps
3-Bromo-2-thiophenecarboxylic acid methyl ester (7.74 g) was dissolved in a mixture of methanol (35 ml) and tetrahydrofuran (35 ml), and 1N aqueous sodium hydroxide (53 ml) was added. The mixture was stirred at room temperature for 2 hours and washed with diethyl ether. The aqueous layer was acidified with 1N hydrochloric acid and extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give 3-bromo-2-thiophenecarboxylic acid (7.05 g) as crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05840917 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-2e768a02cf3442ff911f2d68e5377a5c |
| Source note | uspto-grants-1998_11 |