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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968781Generated: October 30, 2026

Dimethylformamide dimethyl acetal → 2-Nitro-5-phenoxybenzaldehyde

https://huagongshe.com/reaction/1968781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamide dimethyl acetalHCID 78373—
Reactant2-Nitro-5-phenoxytolueneHCID 2728418—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-Nitro-5-phenoxybenzaldehydeHCID 44203082—

Reaction Steps

A mixture of 2-nitro-5-phenoxytoluene (57.3 g, 0.25 mol) prepared in Step A above and dimethylformamide dimethyl acetal (43.1 mL, 0.324 mol) in DMF (259 mL) was heated overnight at 140° C. The mixture was cooled to room temperature, and the solvent was evaporated in vacuo. The residue was dissolved in THF (500 mL) and transferred to a 3L 3-neck flask equipped with an overhead stirrer. The mixture was diluted with 500 mL of water, and NaIO4 (160 g, 0.75 mol) was added in portions (slight exotherm). The mixture was stirred overnight at room temperature. The solids were-filtered and washed well with EtOAc. The filtrate was washed 3× with saturated aqueous NaHCO3 solution, and then dried (MgSO4). The solution was filtered and the solvent was evaporated in vacuo. The crude product was chromatographed (10-40% CH2Cl2:hexane) to yield 2-nitro-5-phenoxy-benzaldehyde as a yellow crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426429B2
Source datasetuspto-grants-2013_04
ORD IDord-2d639e5862c245ca81f8c533e7b8d094
Source noteuspto-grants-2013_04