HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 2-Thiophenecarboxylic acid, 4-bromo-3-methoxy-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl 4-bromo-3-methoxythiophene-2-carboxylate | HCID 2736824 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Thiophenecarboxylic acid, 4-bromo-3-methoxy- | HCID 542267 | 90% |
Reaction Steps
The product from Step A above (22.5 g, 84.36 mmol) was dissolved in 60 mL of tetrahydrofuran and added with 125 mL of a 1.0 M NaOH aqueous solution. The mixture was stirred at room temperature for 4 d, then washed with ether (60 mL×2), acidified to pH ˜2 using a 1.0 M HCl aqueous solution. Solids were precipitated out after acidification, and collected by filtration. The solid was dissolved in methylene chloride-ethyl acetate (˜4:1, v/v). The organic solution was washed with H2O and brine, dried with Na2SO4, and concentrated in vacuo to a light yellow solid, further dried on height vacuum, yielding 17.95 g of 4-bromo-3-methoxy-2-thiophene carboxylic acid (90%, MH+=237.0).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07786149B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-dc9515ace12f42f99dcfe4956070c045 |
| Source note | uspto-grants-2010_08 |