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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108941Generated: October 30, 2026

2,4-Dichlorobenzyl chloride → HCID 16202559, compound

https://huagongshe.com/reaction/2108941

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dichlorobenzyl chlorideHCID 7212—
ReactantPotassium CarbonateHCID 11430—
Reactantmethyl 1H-indazole-3-carboxylateHCID 657476—
SolventAcetoneHCID 180—
SolventDichloromethaneHCID 6344—
ProductHCID 16202559HCID 16202559—

Reaction Conditions

Temperature70 °C

Reaction Steps

Next, a mixture of methyl indazole-3-carboxylate (2.05 g, 11.4 mmol), 2,4-dichlorobenzyl chloride (3.35 mL, 12.54 mml), and K2CO3 (7.0 g, 50 mmol) in acetone (22 mL) was refluxed overnight at a temperature of 70° C. The reaction mixture was cooled to room temperature, filtered, and the residue was washed with acetone. The combined filtrate was concentrated under vacuum (rotovapor). The solid thus obtained was dissolved in CH2Cl2 and filtered to remove any undissolved solid. The solution was then concentrated, diluted with hexane and left in the refrigerator overnight. The precipitated solid was then filtered, washed with a mixture of hexane/ethyl acetate (9:1) to yield the pure product as a white solid. Yield=3.5 g (89%); m.p.=144°-146° C.; 1H NMR (400 MHz, CDCl3) δ 8.31 (d, J=8.8 Hz, 1H), 7.39-7.47 (m, 4H), 7.12 (d, J=8.8 Hz, 1H), 6.71 (d, J=8.8 Hz, 1H), 5.81 (s, 2H), 4.11 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514463B2
Source datasetuspto-grants-2009_04
ORD IDord-d18e2a33a871474aa1c1bc97d4c3793a
Source noteuspto-grants-2009_04