HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11434Generated: October 30, 2026
Ethyl Acetate → 2-(Adamantan-1-yl)-N-methylethan-1-amine
https://huagongshe.com/reaction/11434
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 610088 | HCID 610088 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(Adamantan-1-yl)-N-methylethan-1-amine | HCID 35996 | 66% |
Reaction Steps
A solution of 1-adamantaneacetic acid N-methylamide (1.54 g, 7.45 mmol) in tetrahydrofuran (15.0 ml) was added dropwise to a solution of lithium aluminum hydride (569 mg, 15.0 mmol) in diethyl ether (34.0 ml) under ice-cooling over five minutes. The mixture was refluxed for six hours and then stirred under ice-cooling again. Ethyl acetate was added to the reaction mixture to treat excess lithium aluminum hydride, and then the whole was extracted with 1 N hydrochloric acid (50 ml) twice. A 4 N aqueous sodium hydroxide solution was added to the extract to basify it, and the whole was extracted with diethyl ether (80 ml). The organic layer was washed with a saturated aqueous sodium chloride solution (60 ml) and dried over magnesium sulfate. The solvent was evaporated under reduced pressure to give 890 mg (66%) of the titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07098226B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-77e4a237654146e5910d99caf230f57d |
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| Source note | uspto-grants-2006_08 |
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