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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157963Generated: November 3, 2026

Trimethylsilyl cyanide → HCID 25232593, compound

https://huagongshe.com/reaction/1157963

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl cyanideHCID 82115—
Reactant2-Fluoro-4,5-dimethoxybenzaldehydeHCID 603595—
ReactantYtterbium triflateHCID 2733225—
ReactantHCID 25232416HCID 25232416—
SolventDichloromethaneHCID 6344—
ProductHCID 25232593HCID 25232593—

Reaction Steps

To a mixture of Yb(OTf)3(0.399 g) and dichloromethane (25 mL) there were added (5-amino-2-bromobenzyl)carbamic acid t-butyl ester (Example (3a))(1.95 g), 2-fluoro-4,5-dimethoxybenzaldehyde (1.19 g), MS3A (2.58 g) and trimethylsilyl cyanide (1.29 mL) in that order under a nitrogen atmosphere, and the mixture was stirred at room temperature for 16 hours. The solvent in the mixture was distilled off under reduced pressure, ethyl acetate (200 mL) and water (100 mL) were added to the residue, and after sufficiently shaking the mixture, the organic layer was separated off, washed with saturated aqueous sodium chloride (100 mL) and dried over anhydrous magnesium sulfate. The mixture was filtered to obtain a filtrate, and the solvent in the filtrate was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate-heptane mixture) to obtain the target compound (2.98 g) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807690B2
Source datasetuspto-grants-2010_10
ORD IDord-48fcc1b54b9e4942b45de7d1eb1f4183
Source noteuspto-grants-2010_10