Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2251725Generated: November 3, 2026

4-Nitrobenzaldehyde → HCID 11536760, compound

https://huagongshe.com/reaction/2251725

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrobenzaldehydeHCID 541—
Reactant1,2,4-BenzenetrimethanolHCID 11469297—
CatalystBentoniteHCID 71586775—
SolventTolueneHCID 1140—
ProductHCID 11536760HCID 1153676062.6%

Reaction Steps

10 g of (3,4-bis-hydroxymethylphenyl)methanol (59.4 mmol) (prepared according to Nakazaki, M.; Yamamoto, K. And Miura, Y.; J. Org. Chem., 43(6), (1978), 1041-1044), 100 ml of toluene, 8.98 g of 4-nitrobenzaldehyde (59.4 mmol) and 0.6 g of Montmorillonite KSF (10 mg/mmol) are introduced into a flask equipped with a Dean-Stark. The mixture is heated under reflux for 2 hours 30 minutes. The montmorillonite is filtered off and the reaction medium is allowed to return to room temperature, with stirring. The reaction product crystallizes. After filtration and drying under vacuum at 50° C., 11.2 g of [7-(4-nitrophenyl)-(5H,9H)-6,8-dioxabenzocyclohepten-2-yl]methanol are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07319155B2
Source datasetuspto-grants-2008_01
ORD IDord-4a78cfa256664198abd1b080834c180d
Source noteuspto-grants-2008_01