HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl (4-bromo-2,5-dimethyl-thiophen-3-yl)-oxo-acetate → Ethyl 2-(4-bromo-2,5-dimethylthiophen-3-yl)-2-hydroxyacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl (4-bromo-2,5-dimethyl-thiophen-3-yl)-oxo-acetate | HCID 70818387 | — |
| Reactant | Sodium tetraborohydride | HCID 131720822 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 2-(4-bromo-2,5-dimethylthiophen-3-yl)-2-hydroxyacetate | HCID 70818714 | 89% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a solution of ethyl 2-(4-bromo-2,5-dimethylthiophen-3-yl)-2-oxoacetate (28c) (1 g, 3.56 mmol) in tetrahydrofuran (22.5 mL) and ethanol (5.6 mL) cooled to 0° C. is added sodium tetraborohydride (121.2 mg, 3.20 mmol). The mixture is stirred at 0° C. for 1 hour. The mixture is quenched with HCl (1N) and extracted with ethyl acetate. The organic extract is washed with brine, dried over sodium sulfate, filtered and concentrated to afford the desired alcohol (28d) as a white solid (836 mg, 2.85 mmol, 89%) which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09238026B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-f30e2234a6f64b6dbc1c2ebc1f2daa16 |
| Source note | uspto-grants-2016_01 |