HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37115Generated: October 29, 2026
Trimethylsilyl iodide → HCID 178428623, compound
https://huagongshe.com/reaction/37115
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethylsilyl iodide | HCID 85247 | — |
| Reactant | HCID 19934607 | HCID 19934607 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 178428623 | HCID 178428623 | 80.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05420126 |
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| Source dataset | uspto-grants-1995_05 |
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| ORD ID | ord-11c08331de734e57b5b07e97e4aae238 |
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| Source note | uspto-grants-1995_05 |
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