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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196575Generated: October 31, 2026

Hydrochloric Acid → HCID 67853742, compound

https://huagongshe.com/reaction/1196575

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 67853742HCID 67853742—

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 high pressure liquid chromatography (HPLC) (ethyl acetate/CH3CN/diethylamine; 90:10:1) to give 2.20 g of the pure cis isomer. The hydrochloride was formed in HCl/ether and then recrystallized from methanol/ether to give 1.81 g of cis-5-(dimethylaminomethyl)-4-hydroxy-3-phenyl-4,5,6,7-tetrahydro-1,2-benzisoxazole hydrochloride, m.p. 235°-236° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05114936
Source datasetuspto-grants-1992_05
ORD IDord-7a5b5dfeb12c4176b3d52338a44655e0
Source noteuspto-grants-1992_05