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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489095Generated: October 29, 2026

Chloroiodomethane → HCID 23387571, compound

https://huagongshe.com/reaction/489095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroiodomethaneHCID 11644—
ReactantTetrabutylammonium HydroxideHCID 2723671—
ReactantHCID 23387556HCID 23387556—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 23387571HCID 2338757164.5%

Reaction Steps

To a solution of 5-(N-CBz-L-valyloxy)-4-stearoyloxy-2,2-dimethylvaleric acid (16.0 g, 24 mmol) in dioxane (500 mL), was added dropwise a 40% aqueous solution of tetrabutylammonium hydroxide (14.3 mL). After stirring for 5 min, the solution was evaporated to dryness through co-evaporation with dioxane and toluene. The residue was dissolved in dichloromethane (500 mL) and then chloroiodomethane (17.5 mL, 240 mmol) was added and the solution was stirred for 6 h at room temperature. The solution was concentrated under reduced pressure and the residue was shaken with hexane/ethyl acetate (1:1 v/v, 400 mL). The yellow crystalline solid was filtered off and the filtrate was washed with aqueous solution of sodium thiosulfate (0.1 M) and the filtered through anhydrous sodium sulfate and evaporated to dryness. The residue was column chromatographed (silica gel, 1% MeOH in CH2Cl2), to give 11.0 g of chloromethyl 5-(N-CBz-L-valyloxy)4-stearoyloxy-2,2-dimethylvalerate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06974802B2
Source datasetuspto-grants-2005_12
ORD IDord-d049bf67cfde4842af89b91233100312
Source noteuspto-grants-2005_12