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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 622300Generated: October 25, 2026

Methyl iodide → HCID 13923710, compound

https://huagongshe.com/reaction/622300

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant2-(2-hydroxyethyl)-N-(1,1-dimethylethyl)benzenesulfonamideHCID 13822972—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13923710HCID 13923710—

Reaction Steps

A suspension of 37.0 g of potassium t-butoxide in 400 ml dry tetrahydrofuran was cooled to 0° and a solution of 39.2 g of the product from Example 1 in 300 ml tetrahydrofuran was added dropwise. After the addition was complete, the reaction mixture was stirred at room temperature for 1 hour. After cooling to 0°, 9.3 ml of methyl iodide was added dropwise and the mixture stirred for 15 minutes at 0°. The solution was diluted with ether, washed with water and dried (Na2SO4). Concentration gave a viscous brown oil which was used in the following example, without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04770690
Source datasetuspto-grants-1988_09
ORD IDord-faead79a1ff64b9ca375776ca93da693
Source noteuspto-grants-1988_09