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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1449534Generated: November 1, 2026

Benzaldehyde → N-Trimethylsilylbenzaldimine

https://huagongshe.com/reaction/1449534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantHexamethyldisilazaneHCID 13838—
Reactantn-Butyl lithiumHCID 61028—
SolventTetrahydrofuranHCID 8028—
ProductN-TrimethylsilylbenzaldimineHCID 59549380%

Reaction Steps

In 75 mL of anhydrous THF were added 17.29 mL (75 mmol) of hexamethyldisilazane and 30 mL (75 mmol) of N-butyllithium (2.5M in hexane) at 0° C. under nitrogen. After stirring for one hour, 7.65 mL (75 mmol) of benzaldehyde was added at room temperature, and the mixture was refluxed for 3 hours. Then, 9.52 mL (75 mmol) of freshly distilled trimethylsilyl chloride was added with a syringe. The mixture was refluxed for 2 hours. A white precipitate formed during this process. The reaction mixture was then cooled to room temperature and the liquid layer was transferred with a syringe to a distillation flask under nitrogen. The solvent was evaporated in vacuo, and the oily residue was distilled under reduced pressure (68° C./1 mm Hg) to give pure N-trimethylsilylbenzaldimine as a pale yellow oil (10.6 g, 80%) having the identification data shown below:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05599820
Source datasetuspto-grants-1997_02
ORD IDord-ff385456a65548c2a04f31d43a707372
Source noteuspto-grants-1997_02