HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1866186Generated: November 1, 2026
HCID 24824075, compound → HCID 24824076, compound
https://huagongshe.com/reaction/1866186
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 24824075 | HCID 24824075 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 24824076 | HCID 24824076 | 92.6% |
Reaction Steps
A mixture of 4-[[4-[2-[N-benzyl-N-[(2R)-2-(3-chlorophenyl)-2-hydroxyethyl]amino]ethyl]phenyl](hydroxy)-methyl]phenol (545 mg) in 4N hydrogen chloride in 1,4-dioxane (1.0 ml) was stirred for 5 minutes. The solvent was removed by evaporation. A suspension of the residue in ethanol (2.2 ml) and chlorobenzene (5.2 ml) was hydrogenated over palladium on carbon (10% w/w, 50% wet, 55 mg) under hydrogen atmosphere for 2 hours. The catalyst was filtered off, and the filtrate was evaporated. The residue was diluted with ethyl acetate and saturated sodium biscarbonate solution. The organic layer was separated, washed with brine, dried over magnesium sulfate and evaporated under reduced pressure to give 4-[4-[2-[[(2R)-2-(3-chlorophenyl)-2-hydroxyethyl]amino]ethyl]benzyl]phenol (395 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07629366B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-d367d7ad6942494a8f609d275aeee53e |
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| Source note | uspto-grants-2009_12 |
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