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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443736Generated: October 30, 2026

Hydrochloric Acid → HCID 23465245, compound

https://huagongshe.com/reaction/443736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 12570798HCID 12570798—
SolventWaterHCID 962—
ProductHCID 23465245HCID 2346524539%

Reaction Steps

To a solution of 45 g. (0.12 mole) of N-(β-hydroxy-3-methoxy-α,α-dimethylphenethyl)-3,4-dimethoxybenzeneacetamide in 500 ml. dry tetrahydrofuran is added 200 ml. 1 M (0.2 mole) of BH3 /THF solution over 30 minutes at 0° C. with stirring. After addition, the reaction is allowed to stir overnight at room temperature. Water is added dropwise with caution until effervescence ceases, then 50 ml. more water is added all at once. Aqueous HCl (10%) is added to pH 1.0. Then the acidic reaction mixture is heated at 65° C. for 1 hour to remove most of the tetrahydrofuran and destroy excess BH3. Next, the mixture is cooled with ice and basicified with NH4OH. The mixture is extracted twice with 1 l. ethyl acetate. The combined organic extracts are dried (Na2SO4) and evaporated to dryness in vacuo. The crude hydrochloride is made by dissolving the residue in 250 ml. ethyl acetate and adding a solution of ethyl acetate saturated with dry HCl to pH 2.0. On standing, 25 g. of crude solid is obtained, which is recrystallized from 300 ml. hot isopropanol to give 18.5 g. (39% yield) of α-(1-{[2-(3,4-dimethoxyphenyl)ethyl]amino}-1-methylethyl)-3-methoxybenzenemethanol hydrochloride as a white crystalline solid of analytical purity; m.p. 185°-186° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04261890
Source datasetuspto-grants-1981_04
ORD IDord-76ef08b1b5f3421e86866b3748bb9df6
Source noteuspto-grants-1981_04