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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196576Generated: October 30, 2026

Hydrochloric Acid → HCID 67853753, compound

https://huagongshe.com/reaction/1196576

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 19786539HCID 19786539—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
SolventEther hydrochlorideHCID 10953452—
ProductHCID 67853753HCID 67853753—

Reaction Steps

6,7-Dihydro-5-dimethylaminomethyl-3-phenyl-1,2-benzisoxazol-4(5H)-one hydrochloride (7.5 g) was dissolved in 100 ml ethanol and treated with 5.0 g sodium borohydride. After stirring for 1 hour the reaction mixture was distributed between 5% HCl and ether. The aqueous phase was then made basic with solid sodium bicarbonate and extracted with ether. Concentration under reduced pressure gave the product as a mixture of trans and cis isomers which was chromatographed by preparative HPLC (ethyl acetate/CH3CN/diethylamine; 90:10:1) to give 3.31 g of the pure trans isomer. The hydrochloride was formed in HCl/ether and then recrystallized from methanol/ether to give 2.90 g of trans-5-(dimethylaminomethyl)-4-hydroxy-3-phenyl-4,5,6,7-tetrahydro-1,2-benzisoxazole hydrochloride, m.p. 231°-232° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05114936
Source datasetuspto-grants-1992_05
ORD IDord-0da9f23928ea45118d6ad246c9e773fb
Source noteuspto-grants-1992_05