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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771213Generated: October 30, 2026

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

https://huagongshe.com/reaction/1771213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant(R)-tert-Butyl 3-(aminomethyl)morpholine-4-carboxylateHCID 44182323—
SolventDichloromethaneHCID 6344—
Product(R)-tert-butyl 3-((diethylamino)methyl)morpholine-4-carboxylateHCID 66723762—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of (R)-tert-butyl 3-(aminomethyl)morpholine-4-carboxylate (commercially available, 250 mg, 1.16 mmol) and DCM (7 ml) at 0° C. was treated with acetaldehyde (0.162 ml, 2.89 mmol). The reaction mixture was stirred at 0° C. for 15 minutes and sodium triacetoxyborohydride (612 mg, 2.89 mmol) was added all at once. The resulting mixture was stirred for 24 h and the mixture was diluted with 20 ml of DCM (20 ml) and washed with saturated aq. sodium bicarbonate (20 ml). The organic phase was dried over sodium sulfate, filtered, and concentrate under pressure to give (R)-tert-butyl 3-((diethylamino)methyl)morpholine-4-carboxylate (INTERMEDIATE 90, STEP 1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09248140B2
Source datasetuspto-grants-2016_02
ORD IDord-778e7ce377ba4ba1a4b59d088682ef87
Source noteuspto-grants-2016_02