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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206654Generated: November 5, 2026

Water → Benzyl 2-(1-aminoethyl)morpholine-4-carboxylate

https://huagongshe.com/reaction/2206654

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium AcetateHCID 517165—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantPhenylmethyl 2-acetyl-4-morpholinecarboxylateHCID 18354411—
SolventMeOH tetrahydrofuranHCID 21899815—
ProductBenzyl 2-(1-aminoethyl)morpholine-4-carboxylateHCID 1835434040%

Reaction Steps

To a solution of benzyl 2-acetylmorpholine-4-carboxylate (5.0 g, 19 mmol) in THF/MeOH (1/5, 100 mL) were added AcONH4 (14.6 g, 190 mmol) and NaBH3CN (11.8 g, 190 mmol). The mixture was stirred at room temperature for 50 hr. The mixture was concentrated to give the crude. Water (20 mL) was added and the mixture was extracted by ethyl acetate (60 mL*3), 1N HCl, was added into the combined organic layers. The aqueous layer was concentrated, brought to above pH>8 with 2N NaOH and extracted by ethyl acetate (60 mL*3). The organic layer was washed with brine, dried over sodium sulfate. The mixture was concentrated to give benzyl 2-(1-aminoethyl)morpholine-4-carboxylate (2.0 g, 40%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371331B2
Source datasetuspto-grants-2016_06
ORD IDord-a2677daa602e4c4d8d688d47a9b70c7f
Source noteuspto-grants-2016_06