HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443736Generated: October 30, 2026
Hydrochloric Acid → HCID 23465245, compound
https://huagongshe.com/reaction/443736
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 12570798 | HCID 12570798 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 23465245 | HCID 23465245 | 39% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04261890 |
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| Source dataset | uspto-grants-1981_04 |
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| ORD ID | ord-76ef08b1b5f3421e86866b3748bb9df6 |
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| Source note | uspto-grants-1981_04 |
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