HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111937Generated: November 3, 2026
HCID 22765876, compound → Mabuterol hydrochloride
https://huagongshe.com/reaction/1111937
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 22765876 | HCID 22765876 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Mabuterol hydrochloride | HCID 6917754 | — |
Reaction Steps
0.76 gm of 1-(4'-amino-3'-chloro-5'-trifluoromethyl-phenyl)-2-(N-benzyl-N-tert.butylamino)-ethanol were dissolved in 20 ml of methanol and 1.95 ml of 1N hydrochloric acid, and the solution was hydrogenated in a hydrogenation vessel in the presence of 80 mgm of palladium/coal-catalyst (10%) until 1 mol of hydrogen had been absorbed. Afterwards, the catalyst was removed by filtration, and the filtrate was evaporated to dryness in vacuo. The oily residue was purified by column chromatography (silicagel; chloroform:methanol:concentrated ammonia = 80:20:1 as eluant). The fractions containing the desired substance were combined, and the solvent was removed in vacuo. The remaining crystalline base of the desired compound was converted into its hydrochloride with the calculated quantity of 1.07 N hydrochloric acid in isopropanol, and recrystallized from ethyl acetate/ether. M.p. 205°-207° C. (decomp.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04119710 |
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| Source dataset | uspto-grants-1978_10 |
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| ORD ID | ord-5f62d17c018040ed8ea12e06c83d9746 |
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| Source note | uspto-grants-1978_10 |
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