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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357868Generated: November 4, 2026

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → t-Butyl 3-acetoxy-5-methyl-4-nitrophenylacetate

https://huagongshe.com/reaction/1357868

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
Reactantt-Butyl 3-acetoxy-4-nitrophenylacetateHCID 18188103—
ReactantHCID 178418332HCID 178418332—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Productt-Butyl 3-acetoxy-5-methyl-4-nitrophenylacetateHCID 18188096—

Reaction Steps

A stirred solution of t-butyl 3-acetoxy-4-nitrophenylacetate (8.0 g, Reference Example 18) in tetrahydrofuran (350 mL) at −15° C. under argon was treated dropwise with methyl magnesium chloride solution in diethyl ether (7 mL, 3M) and after 2 hours a further aliquot of methyl magnesium chloride solution in diethyl ether (7 mL, 3M). After stirring for a further 1 hour the reaction mixture was treated with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (10.4 g), then stirred at room temperature overnight, then partially evaporated and then treated with dichloromethane. The mixture was washed with water, then dried and then evaporated. The residue was subjected to flash chromatography on silica eluting with dichloromethane to give the title compound (1.66 g) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06593354B2
Source datasetuspto-grants-2003_07
ORD IDord-c71e9d00b83b43c1afcf78da9f6e3af0
Source noteuspto-grants-2003_07