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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1170633Generated: October 30, 2026

Chloroiodomethane → HCID 23387569, compound

https://huagongshe.com/reaction/1170633

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 acetate 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 numberUS07825238B2
Source datasetuspto-grants-2010_11
ORD IDord-2b9cb4b42ed54e0cbcd34b0d4bdd5e27
Source noteuspto-grants-2010_11