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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489013Generated: October 28, 2026

Chloroiodomethane → chloromethyl 5-(N-CBz-L-valyloxy)-2,2-dimethylvalerate

https://huagongshe.com/reaction/489013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroiodomethaneHCID 11644—
ReactantTetrabutylammonium HydroxideHCID 2723671—
Reactant5-(N-CBz-L-valyloxy)-2,2-dimethylvaleric acidHCID 23387555—
Solvent1,4-DioxaneHCID 31275—
Productchloromethyl 5-(N-CBz-L-valyloxy)-2,2-dimethylvalerateHCID 2338757059.6%

Reaction Steps

To a solution of 5-(N-CBz-L-valyloxy)-2,2-dimethylvaleric acid (5.88 g, 15.5 mmol) in dioxane (100 mL), was added dropwise a 40% aqueous solution of tetrabutylammonium hydroxide (10.1 g). After stirring for 5 min, the solution was evaporated to dryness through co-evaporation with dioxane and toluene. The residue was dissolved in dichloromethane (100 mL) and then chloroiodomethane (11.3 mL, 155 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, 200 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, 1-4% MeOH in CH2Cl2), to give 3.95 g of chloromethyl 5-(N-CBz-L-valyloxy)-2,2-dimethylvalerate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06974802B2
Source datasetuspto-grants-2005_12
ORD IDord-34acf66fb43540259afbef14fd72cd14
Source noteuspto-grants-2005_12