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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37115Generated: October 29, 2026

Trimethylsilyl iodide → HCID 178428623, compound

https://huagongshe.com/reaction/37115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
ReactantHCID 19934607HCID 19934607—
SolventWaterHCID 962—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 178428623HCID 17842862380.8%

Reaction Conditions

Temperature50 °C

Reaction Steps

In 6 ml of carbon tetrachloride was dissolved 0.4 g of 3,4-dihydro-4-[(2-methoxypyridin-3-yl)carbonyl]-2,2-dimethyl-6-nitro-2H-1,4-benzoxazine followed by dropwise addition of 0.26 g of trimethylsilyl iodide. The mixture was heated at 50° C. for 2 hours and, then, cooled. The reaction mixture was diluted with water and extracted with chloroform. The organic layer was dried over anhydrous magnesium sulfate and filtered, the filtrate was concentrated under reduced pressure, and methanol was added to the concentrate for crystallization., Recrystallization from ethyl acetate gave 0.31 g of 3,4-dihydro-4-[(2-hydroxypyridin-3-yl)carbonyl]-2,2-dimethyl-6-nitro-2H-1,4-benzoxazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05420126
Source datasetuspto-grants-1995_05
ORD IDord-11c08331de734e57b5b07e97e4aae238
Source noteuspto-grants-1995_05