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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 583151Generated: October 28, 2026

Methyl 3-(acetoxymethyl)-4-nitrobenzoate → Methyl 3-(hydroxymethyl)-4-nitrobenzoate

https://huagongshe.com/reaction/583151

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 3-(acetoxymethyl)-4-nitrobenzoateHCID 18371998—
SolventMethanolHCID 887—
ProductMethyl 3-(hydroxymethyl)-4-nitrobenzoateHCID 18372008—

Reaction Steps

In a 5-liter three-necked round-bottomed flask equipped with a reflux condenser, overhead stirrer and nitrogen inlet, was placed 318 g of the previously prepared methyl 3-acetoxymethyl-4-nitrobenzoate and 3.2 l of anhydrous methanol. To the resulting solution was bubbled in 40 g of hydrogen chloride and the resulting mixture was refluxed for 3 hours. After cooling to room temperature the solvent was removed using a rotary evaporator yielding 273 g of methyl 3-hydroxymethyl-4-nitrobenzoate as a yellow solid containing traces of methanol, which was used as such in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05929098
Source datasetuspto-grants-1999_07
ORD IDord-ef0ee0219eae46338661525933d0dc48
Source noteuspto-grants-1999_07