HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butanol → HCID 90281979, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 5-Methyl-1-benzothiophene-2-carboxylic acid | HCID 605987 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 90281979 | HCID 90281979 | — |
Reaction Steps
To a solution of 5-methyl-1-benzothiophene-2-carboxylic acid (1.50 g) in N,N-dimethylformamide (10.5 mL) was added 1,1′-carbonyldiimidazole (1.27 g), followed by stirring at room temperature for 2.5 hours. Subsequently, tert-butyl alcohol (1.44 mL) and 1,8-diazabicyclo[5.4.0]undeca-7-ene (1.17 mL) were added thereto, followed by heating at 50° C. for 24 hours. To the reaction mixture was added ethyl acetate, and the organic layer was washed with 1 M hydrochloric acid and a saturated aqueous sodium chloride solution in this order, and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane-ethyl acetate) to obtain tert-butyl 5-methyl-1-benzothiophene-2-carboxylate (1.78 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09199927B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-499ec77f23d144359c9c8faa7dd683ad |
| Source note | uspto-grants-2015_12 |