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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1790797Generated: October 29, 2026

Chloroiodomethane → HCID 23387569, compound

https://huagongshe.com/reaction/1790797

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroiodomethaneHCID 11644—
ReactantTetrabutylammonium HydroxideHCID 2723671—
ReactantHCID 23405699HCID 23405699—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 23387569HCID 23387569—

Reaction Steps

To a solution of 4-(N-benzyloxycarbonyl-L-valyloxy) cyclohexanoic acid (6.6 g, 20 mmole) in 1,4-dioxane (70 ml) was added a 40% solution of tetrabutylammonium hydroxide (11.34 g, 17.5 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 (30.9 g, 175 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 with toluene/acetone. Yield: 4.1 g=55%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071173B2
Source datasetuspto-grants-2006_07
ORD IDord-b9c9d1ce89cf4d4fbc8fd22e5ac47023
Source noteuspto-grants-2006_07