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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440705Generated: October 29, 2026

Methyl iodide → HCID 22404778, compound

https://huagongshe.com/reaction/440705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantO-(2,4,6-Trimethylbenzenesulfonyl)hydroxylamineHCID 11830845—
ReactantHCID 22404807HCID 22404807—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22404778HCID 2240477888.7%

Reaction Steps

A solution of 1.0 gram (0.003 mole) of 3-(4-chloro-2,3-dihydro-2,2-dimethylbenzofuran-7-yl)-6-trifluoromethyluracil (prepared in a manner analogous to that of Example 1, Step G, except that methyl iodide and potassium carbonate were not used) in 30 mL of tetrahydrofuran was stirred, and 0.5 gram (0.003 mole) of potassium carbonate, then 0.7 gram (0.003 mole) of 1-aminooxysulfonyl-2,4,6-trimethylbenzene were added. Upon completion of the addition, the reaction mixture was stirred for one hour and then diluted with water and extracted with three portions of ethyl acetate. The combined extracts were dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure to a residue, which was subjected to column chromatography on silica gel, with 1:4 ethyl acetate:heptane as the eluant. The product-containing fractions were combined and concentrated, yielding 1.0 gram of 1-amino-3-(4-chloro-2,3-dihydro-2,2-dimethylbenzofuran- 7-yl)-6-trifluoromethyluracil. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05521147
Source datasetuspto-grants-1996_05
ORD IDord-c3065e41e1694e8e811004632d0e1330
Source noteuspto-grants-1996_05