HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1408164Generated: October 27, 2026
Aluminium lithium hydride → Methyl(2-(morpholin-4-yl)ethyl)amine
https://huagongshe.com/reaction/1408164
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | tert-butyl N-[2-(morpholin-4-yl)ethyl]carbamate | HCID 58930414 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl(2-(morpholin-4-yl)ethyl)amine | HCID 14979282 | — |
Reaction Steps
Into a 250-mL 3-necked round-bottom flask, was placed a solution of LiAlH4 (7.72 g, 208.65 mmol, 3.00 equiv) in tetrahydrofuran (60 mL). This was followed by the addition of a solution of tert-butyl 2-morpholinoethylcarbamate (16 g, 62.61 mmol, 1.00 equiv, 90%) in tetrahydrofuran (40 mL) dropwise with stirring at 0-5° C. The resulting solution was stirred for 2 h at 70° C. in a oil bath. The reaction was then quenched by the addition of 7.7 mL of water, 7.7 mL of 15% sodium hydroxide, and 23.1 mL of water. The solids were filtered out. The mixture was dried over sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column and eluted with dichloromethane:methanol (0.5% triethylamine) (20:1). This resulted in 4.2 g (42%) of N-methyl-2-morpholinoethanamine as brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08916569B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-16d149a1667d4d08899a7ff3665da080 |
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| Source note | uspto-grants-2014_12 |
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