HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 5-(2-Hydroxyethyl)-3,4-bis(4-methoxyphenyl)isoxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-Isoxazoleacetic acid, 3,4-bis(4-methoxyphenyl)-, methyl ester | HCID 10926250 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-(2-Hydroxyethyl)-3,4-bis(4-methoxyphenyl)isoxazole | HCID 18998922 | 98% |
Reaction Steps
A 5.9 g of sodium borohydride was added to a suspension of 5 g of 5-methoxycarbonylmethyl-3,4-bis(4-methoxyphenyl)isoxazole in 20 ml of methanol, and the resulting mixture was stirred for 1 hour with ice cooling. The reaction mixture was made acidic by portionwise addition of 1N hydrochloric acid and then extracted with 80 ml of ethyl acetate. The organic layer was washed with 20 ml of 1N hydrochloric acid and 20 ml of water in that order, subsequently dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give 4.5 g (yield 98%) of 5-(2-hydroxyethyl)-3,4-bis(4-methoxyphenyl)isoxazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05478856 |
| Source dataset | uspto-grants-1995_12 |
| ORD ID | ord-542b91853e15431fa84b94539c59250a |
| Source note | uspto-grants-1995_12 |