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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266479Generated: November 1, 2026

Methyl iodide → HCID 70051873, compound

https://huagongshe.com/reaction/266479

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHCID 14984048HCID 14984048—
ReactantCID 53628100HCID 178418400—
SolventTetrahydrofuranHCID 8028—
ProductHCID 70051873HCID 7005187332%

Reaction Steps

s-Butyllithium (0.87M in cyclohexane, 20.4 mL) was added dropwise during one hour with stirring at -78° C. to a solution of 4-ethyl-5,7-dimethoxysaccharin (Example 22L, 2.2 g) in tetrahydrofuran (100 mL). After continued stirring at -78° C. for one hour methyl iodide (1.5 mL) was added. Stirring was continued at -78° C. for 15 minutes, the temperature was allowed to rise to room temperature, and the mixture was quenched in water. Aqueous sodium hydroxide (0.5%, 200 mL) was added. The mixture was washed with ethyl acetate (200 mL), acidified with concentrated hydrochloric acid and extracted with ethyl acetate (200 mL). The ethyl acetate extract was washed with aqueous sodium thiosulfate (10%, 50 mL) and saturated aqueous sodium chloride (50 mL), dried over sodium sulfate and stripped of ethyl acetate affording 4-ethyl-5,7-dimethoxy-6-methylsaccharin (0.73 g, 32% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05650422
Source datasetuspto-grants-1997_07
ORD IDord-25b57f4dfb75478796416420b1d1cc29
Source noteuspto-grants-1997_07