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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657104Generated: November 2, 2026

Sodium borohydride → HCID 19786582, compound

https://huagongshe.com/reaction/1657104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 53770206HCID 53770206—
SolventEthanolHCID 702—
SolventAmmonium ChlorideHCID 25517—
ProductHCID 19786582HCID 19786582100%

Reaction Steps

In a 2 liter round-bottomed flask was dissolved 4,5,6,7-tetrahydro-4-oxo-3-phenyl-1,2-benzisoxazol-5-acetic acid ethyl ester (3.0 g) in absolute ethanol (300 ml) at room temperature. Sodium borohydride (6.07 g) was added and the solution was heated to reflux. The solution was cooled to room temperature, then diluted with saturated NH4Cl until a solid appeared. The reaction mixture was basified to pH 9 using 10% NAOH (aq.). The product, an oil, was extracted with ether and the aqueous phase was extracted twice with ether. The combined organic layers were washed with brine, dried (MgSO4), filtered and concentrated to give 2.60 g of 4-hydroxy-5-(2-hydroxyethyl)-3-phenyl-4,5,6,7-tetrahydro-1,2-benzisoxazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05256672
Source datasetuspto-grants-1993_10
ORD IDord-ee67cc65e5a74f9e8a4d304ab1e6c78a
Source noteuspto-grants-1993_10