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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
Reactant2-Chloropropionyl chlorideHCID 111019—
ReactantSodium MethoxideHCID 10942334—
Reactant(r)-2-((4-Methoxybenzyl)amino)propan-1-olHCID 60073967—
SolventWaterHCID 962—
Product(2RS,5R)-4-(4-methoxybenzyl)-5-methyl-2-phenylmorpholin-3-oneHCID 5787003398%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569294B2
Source datasetuspto-grants-2013_10
ORD IDord-8f9395950cc948c39e4aca2a637c8a7e
Source noteuspto-grants-2013_10