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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587937Generated: October 30, 2026

Dimethyl 5-(1-hydroxy-2-nitroethyl)isophthalate → Dimethyl 5-(2-nitrovinyl)isophthalate

https://huagongshe.com/reaction/587937

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl 5-(1-hydroxy-2-nitroethyl)isophthalateHCID 68474723—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
SolventAcetic AnhydrideHCID 7918—
ProductDimethyl 5-(2-nitrovinyl)isophthalateHCID 68478188—

Reaction Conditions

Temperature22 °C

Reaction Steps

To a solution of 2.29 g (8.09 mmol) of dimethyl 5-(1-hydroxy-2-nitroethyl)isophthalate in 50 mL of DCM and 10 mL of acetic anhydride at 22° C. was added 100 mg of 4-dimethylaminopyridine. The solution was stirred at 22° C. for 1.5 h, evaporated and then coevaporated with xylenes (the material darkened slightly). The residue was partitioned between 100 mL of DCM and 50 mL of 1 N HCl. The organic layer was washed with water (50 mL), satd NaHCO3, dried (Na2SO4) and evaporated. The resulting residue was purified by flash chromatography on silica gel eluting with DCM to give dimethyl 5-(2-nitrovinyl)isophthalate as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227918B2
Source datasetuspto-grants-2016_01
ORD IDord-779c57fb7faa4cbc952e9c7e62459a33
Source noteuspto-grants-2016_01