HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569977Generated: October 30, 2026
Phenylethanolamine → HCID 13713311, compound
https://huagongshe.com/reaction/569977
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenylethanolamine | HCID 1000 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 4-(4-Nitrophenyl)butan-2-one | HCID 12235672 | — |
| Reactant | HCID 13713312 | HCID 13713312 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 13713311 | HCID 13713311 | — |
Reaction Steps
A solution of 5.0 g. (25.9 mM) of 2-amino-1-phenylethanol and 3.55 g. (25.9 mM) of methyl 2-(4-nitrophenyl)ethyl ketone in 60 ml. of toluene containing 10 mg. of para-toluenesulfonic acid was heated at reflux for six hours in a flask equipped with a Dean-Stark trap. The water that formed during the reaction was removed via the trap, and then the reaction mixture was cooled to room temperature and concentrated to dryness by evaporation of the solvent under reduced pressure. The solid product that remained was dissolved in 50 ml. of tetrahydrofuran and the solution was heated to reflux. A solution of 13.5 ml. of 2N borane-methyl sulfide complex in tetrahydrofuran was then added dropwise to the reaction mixture, and the mixture was refluxed for an additional ninety minutes. After cooling the reaction mixture to room temperature, it was diluted by addition of diethyl ether saturated with hydrogen chloride. The precipitate that formed was collected by filtration and crystallized from ethanol and diethyl ether to give 3.29 g. of 1-phenyl-2 -[1-methyl-3-(4-nitrophenyl)propylamino]ethanol hydrochloride. M.P. 203-213° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04734437 |
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| Source dataset | uspto-grants-1988_03 |
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| ORD ID | ord-ca764e040de54189bcdbddb9058b57d8 |
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| Source note | uspto-grants-1988_03 |
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