HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butanol → Benzo[b]thiophene-7-acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Benzo[b]thiophene-7-acetonitrile | HCID 11446611 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Benzo[b]thiophene-7-acetamide | HCID 17985839 | — |
Reaction Steps
Add benzo[b]thiophene-7-acetonitrile (1.9 g, 11.0 mmol) to 2-methyl-2-propanol (20 mL). Heat to reflux under nitrogen and add potassium hydroxide pellets (7.4 g, 132 mmol). Stir and reflux under nitrogen for 30 minutes. Pour solution off of the excess potassium hydroxide and dilute with ethyl acetate. Wash with a 1:1 mixture of aqueous saturated sodium chloride, aqueous saturated sodium hydrogen carbonate. Dry the organic phase over anhydrous magnesium sulfate, filter, and concentrate under reduced pressure. Rinse the solid with cold diethyl ether and dry under vacuum to obtain the title compound as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07491716B2 |
| Source dataset | uspto-grants-2009_02 |
| ORD ID | ord-54d8756fdb3d4eab984718bd0720735c |
| Source note | uspto-grants-2009_02 |