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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475432Generated: October 25, 2026

Hydrochloric Acid → HCID 66848046, compound

https://huagongshe.com/reaction/475432

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant(Iodomethyl)cyclopropaneHCID 2763048—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178505794HCID 178505794—
SolventAcetoneHCID 180—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66848046HCID 6684804641%

Reaction Steps

A solution of (E)-N-(2-(6-bromobenzo[d]isoxazol-3-yl)benzylidene)-1,1-bis(4-fluorophenyl)methanamine (Compound 8) (1.34 g) in dry tetrahydrofuran (15 mL) under nitrogen was cooled to −78° C. with stirring and a 1M solution of potassium tert-butoxide in tetrahydrofuran (3.2 mL) added dropwise. Solution turned dark purple. After 20 min (iodomethyl)cyclopropane (1.45 g) was added in one portion and solution slowly warmed to room temperature, stirred at this temperature for 1.5 h then quenched by the addition of water (10 mL) and extracted with ethyl acetate. The organic extract was dried over anhydrous magnesium sulfate and evaporated to leave a dark red gum that was dissolved in acetone (20 mL) and an aqueous 2N HCl solution (15 mL) added and the mixture stirred overnight. The acetone was removed by evaporation and the aqueous solution extracted with dichloromethane. The aqueous solution was made basic with sodium bicarbonate and extracted with dichloromethane, dried over anhydrous magnesium sulfate and evaporated under reduced pressure. SCX purification (eluting with methanol then ammonia in methanol) followed by flash chromatography on silica eluting with 0 to 5% methanol in dichloromethane gave the title product (0.39 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637551B2
Source datasetuspto-grants-2014_01
ORD IDord-52a7c6034f6f4755be6692ee126e69a9
Source noteuspto-grants-2014_01