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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | (R)-tert-Butyl 3-(aminomethyl)morpholine-4-carboxylate | HCID 44182323 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (R)-tert-butyl 3-((diethylamino)methyl)morpholine-4-carboxylate | HCID 66723762 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09248140B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-778e7ce377ba4ba1a4b59d088682ef87 |
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| Source note | uspto-grants-2016_02 |
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