HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672914Generated: October 31, 2026
Hydrochloric Acid → 1-(Diphenylmethyl)-3-[(phenylmethyl)amino]azetidine-3-carboxylic acid
https://huagongshe.com/reaction/1672914
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Benzhydryl-3-benzylaminoazetidine-3-carbonitrile | HCID 21905781 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(Diphenylmethyl)-3-[(phenylmethyl)amino]azetidine-3-carboxylic acid | HCID 21905815 | 88% |
Reaction Steps
To a solution of the 1-(diphenylmethyl)-3-[(phenylmethyl)amino]azetidine-3-carbonitrile (0.80 g, 2.2 mmol), prepared using procedures similar to those described in Kozikowski and Fauq Synlett 1991, 11, 783-4, in ethanol (30 mL) was added solid sodium hydroxide (7.5 mmol), and the resulting mixture was stirred at room temperature for 3 days. Water (6 mL) was added to the reaction mixture and stirring was continued at 90° C. for 2 h. The pH of the reaction mixture was adjusted to 5 with concentrated hydrochloric acid and a white solid precipitated. The mixture was cooled, diluted with water (50 mL) and the solid was collected, washed with water then dried in vacuo to give the 1-(diphenylmethyl)-3-[(phenylmethyl)amino]azetidine-3-carboxylic acid (0.75 g, 88% yield), MS (EI) for C24H24N2O2: 373 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07999006B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-f465af2d91eb474c93dad73c9f51fd5b |
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| Source note | uspto-grants-2011_08 |
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