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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743359Generated: October 27, 2026

Water → methyl 1-benzyl-1H-indazole-3-carboxylate

https://huagongshe.com/reaction/1743359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
Reactantmethyl 1H-indazole-3-carboxylateHCID 657476—
SolventTetrahydrofuranHCID 8028—
Productmethyl 1-benzyl-1H-indazole-3-carboxylateHCID 1056369077%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of sodium hydride (60% in oil, 55 mg, 1.22 mM) in dry THF (10 ml) stirring at 0° C. was added a solution of methyl indazole-3-carboxylate (von Auwers et al, Ber., 52, pg 1345 (1919), 210 mg, 1.22 mM) in dry THF (10 ml). After 10 min benzyl bromide (0.15 ml, 1.22 mM) was added and the solution left stirring at room temperature overnight. Water (2 ml) was added and the solvent removed in vacuo. The residue was partitioned between water and ethyl acetate and the combined organic dried over magnesium sulfate and evaporated. Column chromatography (ethyl acetate/cyclohexane 1:4) provided methyl 1 benzyl-indazole-3-carboxylate as a yellow powder (250 mg, 77%). M.pt. 181° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07009056B2
Source datasetuspto-grants-2006_03
ORD IDord-e5b65c6b4f0b4d19a6c74b200757b4c1
Source noteuspto-grants-2006_03