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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2054391Generated: November 3, 2026

Acetic Acid → 1-Benzhydryl-3-benzylaminoazetidine-3-carbonitrile

https://huagongshe.com/reaction/2054391

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 solids were collected by vacuum filtration, rinsed with a small volume of cold methanol, and then dried, in vacuo, to give I-2A-1c as a solid (3.56 g, 72%): +APcI 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 numberUS07329658B2
Source datasetuspto-grants-2008_02
ORD IDord-8727577979564c5cb7f8ec88f64b6ee3
Source noteuspto-grants-2008_02