HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → [3-(3,4-Difluoro-phenyl)-5-([E]-styryl)-isoxazol-4-yl]-methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-(3,4-Difluoro-phenyl)-5-([E]-styryl)-isoxazole-4-carboxylic acid | HCID 66718191 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [3-(3,4-Difluoro-phenyl)-5-([E]-styryl)-isoxazol-4-yl]-methanol | HCID 66718189 | 73.1% |
Reaction Steps
To a solution of 3-(3,4-difluoro-phenyl)-5-([E]-styryl)-isoxazole-4-carboxylic acid (18 g, 55.0 mmol) and triethylamine (7.7 mL, 55.0 mmol) in THF (450 mL) was added at room temperature a solution of ethyl chloroformate (5.35 mL, 55.0 mmol) in THF (52 mL). After 1 h triethylamine hydrochloride salt was filtered off and washed with a small amount of THF. The solution was added to a solution of sodium borohydride (5.42 g, 138 mmol) in water (52 mL). The mixture was stirred overnight at room temperature. Sodium hydroxide solution (1 N, 180 mL) was added. Extraction with tert-butylmethylether and chromatography (silica, dichloromethane) afforded the title compound (12.6 g, 73%) as a light green solid. MS: m/e=314.2 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08222246B2 |
| Source dataset | uspto-grants-2012_07 |
| ORD ID | ord-6e3ac281b24a4500aa2c2c08801d68de |
| Source note | uspto-grants-2012_07 |