HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 7-Chloro-1-benzothiophene-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl 7-chlorobenzo[b]thiophene-2-carboxylate | HCID 22474203 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 7-Chloro-1-benzothiophene-2-carboxylic acid | HCID 10198242 | — |
Reaction Steps
Methyl 7-chlorobenzo[b]thiophene-2-carboxylate (3 g, 13 mmol) was dissolved is ethanol (15 mL) and treated 5 N sodium hydroxide (5 mL). The reaction was heated at reflux overnight. The volatiles were removed in vacuo and the aqueous residue was acidified to pH 2 using 5 N HCl. The resulting white solid was filtered off, washed well with water and dried in a vacuum oven at 60° C. Yield=2.6 g. MS (M−H)− 210.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07786132B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-fea189dc2932427e8c75b27d77b41223 |
| Source note | uspto-grants-2010_08 |