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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1170616Generated: October 30, 2026

Chloroiodomethane → HCID 53675844, compound

https://huagongshe.com/reaction/1170616

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroiodomethaneHCID 11644—
ReactantTetrabutylammonium HydroxideHCID 2723671—
ReactantHCID 23387363HCID 23387363—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 53675844HCID 53675844—

Reaction Steps

To a solution of 3-(N-benzyloxycarbonyl-L-valyloxy)propanoic acid (5.2 g, 16.08 mmole) in 1,4-dioxane (50 ml) was added a 40% solution of tetrabutylammonium hydroxide (10.43 g, 16.08 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 40 ml dichloromethane and chloroiodomethane (28.4 g. 160 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: 2.2 g=35%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07825238B2
Source datasetuspto-grants-2010_11
ORD IDord-a2f9b97b0bc84204884f69b9ab92abca
Source noteuspto-grants-2010_11