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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1405392Generated: October 25, 2026

Sodium bis(trimethylsilyl)amide → 3-Methyl-4-(oxetan-3-YL)benzonitrile

https://huagongshe.com/reaction/1405392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant3-IodooxetaneHCID 13356686—
Reactant(4-Cyano-2-methyl-phenyl)boronic acidHCID 16218401—
CatalystNickel(II) iodideHCID 26038—
Catalyst(1S,2S)-2-Aminocyclohexanol hydrochlorideHCID 11715205—
SolventEthanolHCID 702—
SolventIsopropanolHCID 3776—
Product3-Methyl-4-(oxetan-3-YL)benzonitrileHCID 6815330965.42%

Reaction Steps

(4-Cyano-2-methyl-phenyl)boronic acid (1.75 g, 10.87 mmol), diiodonickel (102 mg, 0.326 mmol), (1S,2S)-2-aminocyclohexan-1-ol hydrochloride (50 mg, 0.33 mmol) and NaHMDS (2.01 g, 11.0 mmol) were combined in isopropanol (10 mL) under N2 in a pressure vial. A solution of 3-iodooxetane (1.00 g, 5.44 mmol) in isopropanol (1 mL) was added. The vial was immersed in a pre-heated 90° C. oil bath and stirred for 2 h, then cooled, diluted with ethanol (20 mL), filtered over Celite, concentrated, then absorbed onto Celite and purified by silica gel column chromatography (0-60% EtOAc/hexane) to give 3-methyl-4-(oxetan-3-yl)benzonitrile (616 mg, 3.556 mmol, 65.42%) as a white solid. ESI-MS m/z calc. 173.1, found 174.3 (M+1)+; Retention time: 1.09 minutes (3 min run).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916565B2
Source datasetuspto-grants-2014_12
ORD IDord-e1140e27dd8b4332a0632d541dab42c0
Source noteuspto-grants-2014_12