HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 622551Generated: October 27, 2026
Triethylamine → 1-Benzhydryl-N-methylazetidine-3-carboxamide
https://huagongshe.com/reaction/622551
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 1-(Diphenylmethyl)azetidine-3-carboxylic acid | HCID 2735440 | — |
| Reactant | Methylamine hydrochloride | HCID 6364545 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-Benzhydryl-N-methylazetidine-3-carboxamide | HCID 13772849 | 114.6% |
Reaction Steps
To a solution of 7.5 g (28 mmole) of 1-(diphenylmethyl)azetidine-3-carboxylic acid in 75 ml of acetonitrile was added 6.0 g (37 mmole) of 1,1'-carbonyldiimidazole. The reaction was heated at 60° C. for two hours and successively treated with 3.11 g (30.8 mmole) of triethylamine and 2.08 g (30.8 mmole) of methylamine hydrochloride. The reaction was stirred at 60° C. for an additional hour, the solvent evaporated in vacuo, and the residue dissolved in chloroform. After washing with water and drying over magnesium sulfate, the chloroform layer was evaporated in vacuo to give 9.0 g of 1-(diphenylmethyl)-N-methyl-3-azetidinecarboxamide, mp 103°-107° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04771054 |
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| Source dataset | uspto-grants-1988_09 |
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| ORD ID | ord-e0628356b66b4464abbba721d9c74788 |
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| Source note | uspto-grants-1988_09 |
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