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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301231Generated: October 30, 2026

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

https://huagongshe.com/reaction/2301231

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 numberUS06500405B1
Source datasetuspto-grants-2002_12
ORD IDord-8cd96c2675c74063b48b53751fc0bb8b
Source noteuspto-grants-2002_12