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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 512019Generated: October 25, 2026

Saccharin → N-(6-tert-Butyldimethylsilyloxy-hexyl)saccharin

https://huagongshe.com/reaction/512019

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSaccharinHCID 5143—
ReactantSodium hydrideHCID 24758—
Reactant(6-Bromohexyloxy)-tert-butyldimethylsilaneHCID 4260352—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductN-(6-tert-Butyldimethylsilyloxy-hexyl)saccharinHCID 2501886845%

Reaction Steps

To a solution of saccharin (92 mg, 0.5 mmol) in anhydrous DMF (4 mL), at room temperature, under a nitrogen atmosphere, was added NaH (60% dispersion in mineral oil, 21 mg, 0.52 mmol). The mixture was stirred at the same temperature for additional 15 min, a solution of (6-bromohexyloxy)-tert-butyldimethylsilane (177 mg, 0.6 mmol) in DMF (1 mL) was added and the resulting mixture microwaved at 150° C. for 10 min. The reaction mixture was cooled to room temperature and diluted with water (5 mL) and AcOEt (10 mL). The organic layer was separated and the aqueous layer extracted with AcOEt (2×10 mL). The combined organic layer was washed with brine, dried (MgSO4) and the solvent removed in vacuum. The residue was purified by flash column chromatography on silica gel (20% ethyl acetate-petroleum ether) to give 83.8 (89 mg, 45% yield), as a viscous liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102622B2
Source datasetuspto-grants-2015_08
ORD IDord-b27bcf4747144841a9e1fa95fccda40d
Source noteuspto-grants-2015_08