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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82216Generated: October 30, 2026

Water → Ethyl (6-chloro-1-methyl-1H-indazol-3-yl)acetate

https://huagongshe.com/reaction/82216

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178470796HCID 178470796—
SolventTetrahydrofuranHCID 8028—
ProductEthyl (6-chloro-1-methyl-1H-indazol-3-yl)acetateHCID 70847731100%

Reaction Steps

Sodium hydride (24 mg, 0.602 mmol, 60% in oil) was added to ethyl (6-chloro-1H-indazol-3-yl)acetate (Preparation 168, 120 mg, 0.502 mmol) in THF (4 mL) at 0° C. and the mixture was stirred for 30 minutes. Then iodomethane (0.09 mL, 1.508 mmol) was added. The mixture was stirred at room temperature for 30 mins then water (4 mL) was added. The mixture was evaporated in vacuo and the aqueous residue was acidified with aqueous HCl (6 M). This was extracted with ethyl acetate (10 mL) and the organic phase was dried over sodium sulphate and evaporated in vacuo to afford the title compound as a white solid in 100% yield, 150 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846698B2
Source datasetuspto-grants-2014_09
ORD IDord-577d074b4c464056aa9e8b64afcdfa8d
Source noteuspto-grants-2014_09