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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019063Generated: November 1, 2026

Chloroiodomethane → HCID 22035697, compound

https://huagongshe.com/reaction/1019063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroiodomethaneHCID 11644—
ReactantTetrabutylammonium HydroxideHCID 2723671—
Reactant4-(4-methoxybenzyloxy) benzoic acidHCID 11334401—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 22035697HCID 22035697—

Reaction Steps

To a solution of 4-(4-methoxybenzyloxy)benzoic acid (5.16 g, 20 mmole) in 100 ml 1,4-dioxane was added a 40% solution of tetrabutylammonium hydroxide (14.27 g, 22 mmole) and the mixture was stirred 2 hours at room temperature. The mixture was evaporated under reduced pressure and co-evaporated two times with 1,4-dioxane and two times with toluene. The dried product was dissolved in 60 ml dichloromethane and iodochloromethane (35.3 g 200 mmole) was added. The solution was stirred for two days at room temperature and evaporated under reduced pressure. About 100 ml ethyl actate was added and the organic phase washed twice with water, dried with sodium sulfate and evaporated under reduced pressure. The product was isolated by silica gel column chromatography. Yield: 4.48 g=73%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06486183B1
Source datasetuspto-grants-2002_11
ORD IDord-d74fbedeb722425fae6757837484a44a
Source noteuspto-grants-2002_11