Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1170613Generated: October 28, 2026

Chloroiodomethane → HCID 54441965, compound

https://huagongshe.com/reaction/1170613

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroiodomethaneHCID 11644—
ReactantTetrabutylammonium HydroxideHCID 2723671—
ReactantHCID 53966558HCID 53966558—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 54441965HCID 54441965—

Reaction Steps

To a solution of 3-(N-benzyloxycarbonyl-valyloxy)benzoic acid (7.42 g, 20 mmole) in 1,4-dioxane (100 ml) was added a 40% solution of tetrabutylammonium hydroxide (12.97 g, 20 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 dichloromethane (50 ml) and chloroiodomethane (35.3 g, 200 mmole) was added. The solution was stirred for two days at room temperature and evaporated under reduced pressure. Ethyl acetate (100 ml) 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: 3.8 g=45%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07825238B2
Source datasetuspto-grants-2010_11
ORD IDord-bb026cecb95640fba7ac0f8ac3a7eb24
Source noteuspto-grants-2010_11