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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182341Generated: October 31, 2026

HCID 22477758, compound → HCID 22477919, compound

https://huagongshe.com/reaction/2182341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22477758HCID 22477758—
ReactantHCID 178418287HCID 178418287—
SolventDichloromethaneHCID 6344—
ProductHCID 22477919HCID 2247791947.7%

Reaction Steps

4 Å molecular sieves are added to a solution of 45.7 mg of (2-benzyl-5-ethoxy-2H-pyrazol-3-yl)methanol in 0.5 ml of dichloromethane, followed by addition of 43.1 mg of pyridinium chlorochromate. After 20 hours at a temperature in the region of 20° C., the reaction mixture is filtered through Celite. The insoluble material formed is rinsed with ethyl acetate and then with dichloromethane. The filtrate is washed with water. After separation of the phases by settling, the aqueous phase is re-extracted with dichloromethane. The organic phases are combined, dried over magnesium sulphate, filtered and then concentrated under reduced pressure. 21.6 mg of 2-benzyl-5-ethoxy-2H-pyrazole-3-carboxaldehyde are thus obtained in the form of a brown lacquer, the characteristics of which are as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897208B2
Source datasetuspto-grants-2005_05
ORD IDord-6b4af1eb44584f56bbac179151e3cc5a
Source noteuspto-grants-2005_05