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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1476311Generated: October 26, 2026

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

https://huagongshe.com/reaction/1476311

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 numberUS09018381B2
Source datasetuspto-grants-2015_04
ORD IDord-c3c371146f60479dad0232dfb242e8fa
Source noteuspto-grants-2015_04