HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 978571Generated: October 29, 2026
Water → 1-(diphenylmethyl)-N-methyl-3-azetidinemethanamine
https://huagongshe.com/reaction/978571
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Benzhydryl-N-methylazetidine-3-carboxamide | HCID 13772849 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(diphenylmethyl)-N-methyl-3-azetidinemethanamine | HCID 14280897 | 93.9% |
Reaction Steps
To a suspension of 3.2 g (85 mmole) of lithium aluminum hydride in 50 ml of dry tetrahydrofuran was added dropwise, a solution of 8.5 g (28 mmole) of 1-diphenylmethyl-N-methyl-3-azetidinecarboxamide in 50 ml of dry tetrahydrofuran. After the addition was complete, the reaction was refluxed for two hours, cooled to room temperature, and decomposed by the successive addition of 3.4 ml of water, 3.4 ml of 15% aqueous sodium hydroxide and 10.2 ml of water, titrating the final water addition to give a granular precipitate. The inorganic precipitate was removed by filtration, washed with tetrahydrofuran, and evaporated in vacuo. The residue was dissolved in chloroform, dried over magnesium sulfate, filtered, and evaporated in vacuo to give 7.0 g of 1-(diphenylmethyl)-N-methyl-3-azetidinemethanamine as a heavy syrup. This was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04665079 |
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| Source dataset | uspto-grants-1987_05 |
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| ORD ID | ord-f7ce6f345eea4151af401ad1d5a9fa55 |
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| Source note | uspto-grants-1987_05 |
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