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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2287657Generated: October 30, 2026

Water → HCID 57479269, compound

https://huagongshe.com/reaction/2287657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant6-NitroveratraldehydeHCID 88505—
ReactantHCID 18705686HCID 18705686—
ReactantHCID 178418582HCID 178418582—
SolventDimethylformamideHCID 6228—
ProductHCID 57479269HCID 5747926955.3%

Reaction Steps

At room temperature, NaOCH3 (335 mg, 6.19 mmol) was added to a solution of 1,3-dioxan-2-ylmethyltributylphosphoniumbromide (C. Spangler; R. McCoy, Synthetic communications, 18, 51, (1988)) (5.17 ml, 1 M in DMF, 5.71 mmol) and 4,5-dimethoxy-2-nitro-benzaldehyde (1.25 g, 4.76 mmol) in DMF (20 ml). After heating the mixture at 50° for overnight, the mixture was poured over water, and extracted with ether, washed with brine and dried over MgSO4. The solvent was evaporated and the residue was dissolved in THF (100 ml) and treated with 2 N HCl (50 ml). After stirring the mixture at room temperature for 2 h, the THF was evaporated, and the yellow solid was filtered, and suspended in ether/ethylacetate 4:1. The suspension stirred at room temperature for 1 h, filtered and washed with ether to afford (E)-3-(4,5-dimethoxy-2-nitro-phenyl)-propenal (624 mg, 55%) as a yellow solid, m.p. 103-105°. IR (KBr): 1689, 1605 cm-1. MS (EI): 237 (M).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06084120
Source datasetuspto-grants-2000_07
ORD IDord-9ce58923aa884971a77f4b0e573434cd
Source noteuspto-grants-2000_07