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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1681472Generated: November 2, 2026

Hexamethyldisilazane → HCID 19806769, compound

https://huagongshe.com/reaction/1681472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexamethyldisilazaneHCID 13838—
ReactantHCID 19806692HCID 19806692—
SolventAcetonitrileHCID 6342—
ProductHCID 19806769HCID 19806769—

Reaction Steps

To 3-ethoxy-4-bromo-5-t-butyloxycarbonylisothiazole-1,1-dioxide (340 mg, 1.0 mmol) in 5 ml of dry acetonitrile was added hexamethyldisilazane (242 mg, 1.5 mmol) and the solution was stirred at reflux for 7 hours. The reaction mixture was evaporated in vacuo and the residue was refluxed in 10 ml of ethanol for 3/4 hr. Removal of the ethanol in vacuo gave a crude oil which was chromatographed on silica gel. The product was recovered as a viscous yellow oil (210 mg). Trituration in petroleum ether gave a yellow solid, m.p. 128°-130° C. Mass spectral analysis confirmed the structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05171860
Source datasetuspto-grants-1992_12
ORD IDord-7e45e6d7bb7146eb9bab4e4877858c5f
Source noteuspto-grants-1992_12