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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260923Generated: October 30, 2026

Phosgene → (R,S)-1-(3,4-(Methylenedioxy)-6-nitrophenyl)ethyl chloroformate

https://huagongshe.com/reaction/2260923

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
Reactant1-(6-Nitro-2H-1,3-benzodioxol-5-yl)ethan-1-olHCID 10932738—
ReactantDiethylether hexaneHCID 21584099—
SolventTetrahydrofuranHCID 8028—
Product(R,S)-1-(3,4-(Methylenedioxy)-6-nitrophenyl)ethyl chloroformateHCID 459086185%

Reaction Steps

Phosgene (500 mL of 20% w/v in toluene from Fluka: 965 mmole; 4 eq.) was added slowly to a cold, stirring solution of 50 g (237 mmole; 1 eq.) of 1-(4,5-methylenedioxy-2-nitrophenyl)ethanol in 400 mL dry THF. The solution was stirred overnight at ambient temperature at which point TLC.(20% Et2O/hexane) indicated >95% conversion. The mixture was evaporated (an oil-less pump with downstream aqueous NaOH trap is recommended to remove the excess phosgene) to afford a viscous brown oil. Purification was effected by flash chromatography on a short (9×13 cm) column of silica gel eluted with 20% Et2O/hexane. Typically 55 g (85%) of the solid yellow MeNPOC-Cl is obtained by this procedure. The crude material has also been recrystallized in 2-3 crops from 1:1′ether/hexane. On this scale, ˜100 ml is used for the first crop, with a few percent THF added to aid dissolution, and then cooling overnight at −20° C. (this procedure has not been optimized). The product should be stored desiccated at −20° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846659B2
Source datasetuspto-grants-2010_12
ORD IDord-98d4c1f85d6e4e5783ce7b05ff091e13
Source noteuspto-grants-2010_12