HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1929459Generated: October 25, 2026
Hydrochloric Acid → (RS)-5-(3-amino-phenyl)-5-methyl-morpholin-3-one hydrochloride
https://huagongshe.com/reaction/1929459
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | (RS)-5-[3-(benzhydrylidene-amino)-phenyl]-5-methyl-morpholin-3-one | HCID 58155203 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | (RS)-5-(3-amino-phenyl)-5-methyl-morpholin-3-one hydrochloride | HCID 66931504 | 88% |
Reaction Steps
A solution of (RS)-5-[3-(benzhydrylidene-amino)-phenyl]-5-methyl-morpholin-3-one (5.62 g, 15 mmol) in dioxane (75 ml) was cooled to 15° C. and treated dropwise with 1 N hydrochloric acid (18 ml). The reaction mixture was stirred at room temperature overnight. For the workup, the reaction mixture was evaporated at reduced pressure, and the residue was portioned between diethylether (120 ml) and 1 N hydrochloric acid (20 ml). The aqueous phase was separated and washed with diethylether (120 ml). This procedure was repeated twice. The combined aqueous layers were evaporated at reduced pressure, and 3.27 g (88% of theory) of (RS)-5-(3-amino-phenyl)-5-methyl-morpholin-3-one hydrochloride were obtained as a yellowish solid used in the next step without further purification. Mass (calculated) C11H15ClN2O2 [242.707]; (found) [M+H]+=207.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08188079B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-ac155ce95c60482a82b9faff1c9adfc1 |
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| Source note | uspto-grants-2012_05 |
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