HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2409806Generated: November 1, 2026
Aluminium lithium hydride → Methyl(2-(morpholin-4-yl)ethyl)amine
https://huagongshe.com/reaction/2409806
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 | 46.5% |
Reaction Steps
To a solution of LiAlH4 (7.72 g, 208.65 mmol, 3.00 equiv) in tetrahydrofuran (60 mL) at 0-5° C. was added dropwise a solution of tert-butyl 2-morpholinoethylcarbamate (16 g, 62.61 mmol, 1.00 equiv, 90%) in tetrahydrofuran (40 mL). The resulting solution was then stirred for 2 h at 70° C. in an 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) to afford 4.2 g (42%) of N-methyl-2-morpholinoethanamine as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08815910B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-17423fb730fd45ae98f29fcf3b672bfa |
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| Source note | uspto-grants-2014_08 |
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