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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667784Generated: October 30, 2026

Trimethyl orthoformate → 1-Dimethoxymethyl-5-fluoro-2-methoxy-4-nitro-benzene

https://huagongshe.com/reaction/1667784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl orthoformateHCID 9005—
ReactantSodium BicarbonateHCID 516892—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant5-Fluoro-2-methoxy-4-nitrobenzaldehydeHCID 86222845—
SolventMethanolHCID 887—
Product1-Dimethoxymethyl-5-fluoro-2-methoxy-4-nitro-benzeneHCID 67426673—

Reaction Steps

A mixture of 0.210 g (1.06 mmole) of 5-fluoro-2-methoxy-4-nitro-benzaldehyde (IV.46c), 1 mL of trimethylorthoformate, 0.025 g of p-toluenesulfonic acid monohydrate and 5 mL of methanol was heated at reflux for one hour. The mixture was cooled, neutralized by addition of saturated sodium bicarbonate solution and concentrated under reduced pressure. The residue was partitioned between ethyl acetate and saturated sodium bicarbonate solution. The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to give 0.243 g of 1-dimethoxymethyl-5-fluoro-2-methoxy-4-nitro-benzene (IV.46d) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044213B2
Source datasetuspto-grants-2011_10
ORD IDord-7c1f0805e1364af38007b03c0827af1c
Source noteuspto-grants-2011_10