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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657088Generated: November 3, 2026

Hydrochloric Acid → HCID 67853753, compound

https://huagongshe.com/reaction/1657088

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 numberUS05256672
Source datasetuspto-grants-1993_10
ORD IDord-836800f103c24ea8adbed812f5168d13
Source noteuspto-grants-1993_10