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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1438335Generated: November 2, 2026

Dimethylformamide → 5-chloro-3-ethyl-1-methyl-1h-pyrazole-4-carbaldehyde

https://huagongshe.com/reaction/1438335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantHCID 178436950HCID 178436950—
SolventDichloromethaneHCID 6344—
Product5-chloro-3-ethyl-1-methyl-1h-pyrazole-4-carbaldehydeHCID 275750862%

Reaction Conditions

Temperature0 °C

Reaction Steps

POCl3 (236.88 g, 1.543 mol, 144 mL) was added dropwise at 0° C. to DMF (59 g, 0.808 mol). The reaction mixture was then diluted with dichloromethane (200 mL), and: 3-ethyl-1-methyl-1H-pyrazol-5-ol (84.5 g, from Step 1) was added while stirring at 0° C. The mixture was refluxed for 3 h and then stirred overnight at room temperature. After this, ice-cold water (500 mL) was added rapidly at 0° C. to the reaction mixture in order to decompose the formylation agent. The organic layer was separated, and the aqueous phase extracted with chloroform several times. The organic layers were then washed with K2CO3 solution to obtain a weak alkaline media, dried over Na2SO4 and evaporated to give 51.2 g of an oily substance. The residual reaction mass was neutralized with K2CO3 to obtain a weak acidic media and extracted with chloroform. The combined extracts were concentrated and the residue purified by chromatography (dichloromethane) on a silica gel to give 71.3 g (62%) of the title product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622605B2
Source datasetuspto-grants-2009_11
ORD IDord-092ff31d4d794875a1cea9487fd7e363
Source noteuspto-grants-2009_11