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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantBenzylamineHCID 7504—
ReactantSodium CyanideHCID 8929—
Reactant1-(Diphenylmethyl)azetidin-3-oneHCID 3735558—
SolventMethanolHCID 887—
Product1-Benzhydryl-3-benzylaminoazetidine-3-carbonitrileHCID 2190578172%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129239B2
Source datasetuspto-grants-2006_10
ORD IDord-a8dece8dd24b48f68cefb32b7394f4ab
Source noteuspto-grants-2006_10