HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045699Generated: October 26, 2026
Hydrochloric Acid → (2RS,5R)-4-(4-methoxybenzyl)-5-methyl-2-phenylmorpholin-3-one
https://huagongshe.com/reaction/1045699
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Chloropropionyl chloride | HCID 111019 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | (r)-2-((4-Methoxybenzyl)amino)propan-1-ol | HCID 60073967 | — |
| Solvent | Water | HCID 962 | — |
| Product | (2RS,5R)-4-(4-methoxybenzyl)-5-methyl-2-phenylmorpholin-3-one | HCID 57870033 | 98% |
Reaction Steps
2-Chloro-2-methylacetyl chloride (8.4 g, 40.0 mmol) was added to a solution of (2R)-2-(4-methoxybenzylamino)-propan-1-ol (7.79 g, 39.9 mmol) and triethylamine (4.5 g, 44.5 mmol) in tetrahydrofuran (100 ml) and the solution was stirred for one hour. The solution was cooled at 0° C. and 28% sodium methoxide in methanol solution (15.4 g, 79.8 mol) was added. When the reaction was complete (checked by thin layer chromatography), excess reagent was decomposed by the addition of water and pH was adjusted to 5-6 with 3N aqueous hydrochloric acid. The solution was partitioned between water and chloroform. The organic layer was washed with brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent; 30-50% ethyl acetate in hexane) to afford (2RS,5R)-4-(4-methoxybenzyl)-5-methyl-2-phenylmorpholin-3-one (12.2 g, 39.1 mmol, 98%) as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08569294B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-8f9395950cc948c39e4aca2a637c8a7e |
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| Source note | uspto-grants-2013_10 |
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