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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771206Generated: October 26, 2026

Acetaldehyde → (S)-tert-butyl 3-((diethylamino)methyl)morpholine-4-carboxylate

https://huagongshe.com/reaction/1771206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant(S)-tert-Butyl 3-(aminomethyl)morpholine-4-carboxylateHCID 44182324—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product(S)-tert-butyl 3-((diethylamino)methyl)morpholine-4-carboxylateHCID 66723823—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of (S)-tert-butyl 3-(aminomethyl)morpholine-4-carboxylate (1.0 g, 4.62 mmol) in MeOH (15 ml) was treated with acetaldehyde (0.204 g, 4.62 mmol). The reaction mixture was stirred at 0° C. for 15 minutes and sodium triacetoxyborohydride (2.450 g, 11.56 mmol) was added all at once. The resulting mixture was stirred for 24 h and the mixture was diluted with DCM (15 ml) and washed with saturated aq. sodium bicarbonate (15 ml). The organic phase dried over sodium sulfate, filtered, and concentrated under pressure to give a residue which was purified by column chromatography (ISCO, 12 g silica gel column, eluting with 0→20% MeOH in DCM) to give (S)-tert-butyl 3-((diethylamino)methyl)morpholine-4-carboxylate (INTERMEDIATE 86, STEP 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09248140B2
Source datasetuspto-grants-2016_02
ORD IDord-2969e99b97524891a8f9e1a38c7cf4e1
Source noteuspto-grants-2016_02