HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246795Generated: October 30, 2026
Acetic Acid → 1-Benzhydryl-3-benzylaminoazetidine-3-carbonitrile
https://huagongshe.com/reaction/1246795
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 1-(Diphenylmethyl)azetidin-3-one | HCID 3735558 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-Benzhydryl-3-benzylaminoazetidine-3-carbonitrile | HCID 21905781 | 72% |
Reaction Steps
To a solution of 1-benzhydrylazetidin-3-one (3.3 g, 14 mmol) in methanol (35 ml) was added benzylamine (1.6 ml, 15 mmol) and then acetic acid (0.88 ml, 15 mmol) at room temperature. After stirring for 45 minutes, solid NaCN (0.76 g, 15 mmol) was added in portions over 2 minutes and the mixture was heated to reflux overnight. The reaction, which now contained a precipitate, was cooled and then stirred at room temperature. The solid were collected by vacuum filtration, rinsed with a small volume of cold methanol, and then dried, in vacuo, to give I-(13A-9)a as a solid (3.56 g, 72%): +ACPI MS (M+1) 354.4; 1H NMR (400 MHz, CD3OD) δ 7.40 (d, J=7.5 Hz, 4H), 7.35 (d, J=7.5 Hz, 2H), 7.31–7.20 (m, 7H), 7.16 (t, J=7.3 Hz, 2H), 4.44 (s, 1H), 3.76 (s, 2H), 3.48 (d, J=8.3 Hz, 2H), 3.05 (d, J=8.3 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07129239B2 |
|---|
| Source dataset | uspto-grants-2006_10 |
|---|
| ORD ID | ord-a8dece8dd24b48f68cefb32b7394f4ab |
|---|
| Source note | uspto-grants-2006_10 |
|---|