Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260747Generated: October 30, 2026

Hydrochloric Acid → 5-(2-Hydroxyethyl)-3,4-bis(4-methoxyphenyl)isoxazole

https://huagongshe.com/reaction/2260747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
Reactant5-Isoxazoleacetic acid, 3,4-bis(4-methoxyphenyl)-, methyl esterHCID 10926250—
SolventMethanolHCID 887—
Product5-(2-Hydroxyethyl)-3,4-bis(4-methoxyphenyl)isoxazoleHCID 1899892298%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05478856
Source datasetuspto-grants-1995_12
ORD IDord-542b91853e15431fa84b94539c59250a
Source noteuspto-grants-1995_12