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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586090Generated: October 29, 2026

Hydrochloric Acid → 3-Amino-1-morpholin-4-ylpropan-1-one;2-phenylacetic acid

https://huagongshe.com/reaction/586090

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPhenylacetic AcidHCID 999—
Reactant3-Amino-1-(morpholin-4-yl)propan-1-oneHCID 6504250—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
Product3-Amino-1-morpholin-4-ylpropan-1-one;2-phenylacetic acidHCID 86585919—

Reaction Steps

A reactor is charged with 3-amino-1-morpholin-4-yl-propan-1-one; hydrochloride (765 mmol). MeOH (380 mL) is added, and the mixture is stirred vigorously at room temperature for ca. 10 minutes. MtBE (380 mL) is added and the resulting slurry is cooled to −10° C., where a 25% (w/w) MeOH solution of NaOMe (765 mmol) is added slowly via addition funnel at such a rate as to maintain an internal temperature of ca. −10° C. The resulting suspension is stirred vigorously under a N2 atmosphere as it is allowed to warm to 0° C. Solids are removed via filtration, rinsing with additional MtBE (50 mL). Solvent is removed in vacuo to provide the free base as a crude oil that is taken up in MtBE (600 mL). The mixture is cooled with vigorous agitation to ca. 0° C., where phenylacetic acid (765 mmol) is added slowly as a solution in MtBE (300 mL). The reaction mixture is stirred an additional 10 minutes after complete addition, during which time the product precipitates out of solution. The solids are collected via filtration, washed with additional MtBE (100 mL) and dried under vacuum at ≦40° C. to provide 3-amino-1-morpholin-4-yl-propan-1-one; compound with phenylacetic acid (191 g). This material is carried on to subsequent steps without further purification, or optionally, it can be re-precipitated from MtBE.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06933393B2
Source datasetuspto-grants-2005_08
ORD IDord-3914e66d820d40e1960bef450f15c76a
Source noteuspto-grants-2005_08