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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280184Generated: October 31, 2026

Dichloromethane → 3,5-dinitrobenzaldehyde

https://huagongshe.com/reaction/1280184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant3,5-Dinitrobenzyl alcoholHCID 116978—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product3,5-dinitrobenzaldehydeHCID 171230389%

Reaction Conditions

Temperature-65 °C

Reaction Steps

To a solution of oxalylchloride (26 ml, 0.30 mol) in CH2Cl2 (600 ml) DMSO (43 ml, 0.60 mol) was added, maintaining the temperature between −50° C. and −65° C. To the reaction solution was then added 3,5-dinitrobenzyl alcohol (50g), in THF (100 ml), maintaining the temperature between −50° C. and −65° C. The reaction mixture was stirred at −65° C. for 30 minutes and then triethylamine (170 ml) was added at −50° C. and −65° C. The reaction temperature was then adjusted to room temperature and H2O (800 ml) was added. The organic phase was washed with sat. NaHCO3 (500 ml), 5 times with diluted HCl (300 ml) and finally brine. The organic phase was then dried over MgSO4 and the volatile solvents were removed at reduced pressure. The crude product was then triturated with heptane, which gave 45.8 g (89%) of 3,5-dinitrobenzaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06448442B1
Source datasetuspto-grants-2002_09
ORD IDord-559a51bd6d514a9ea7d285f4b0c5ae81
Source noteuspto-grants-2002_09