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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | methyl 1H-indazole-3-carboxylate | HCID 657476 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | methyl 1-benzyl-1H-indazole-3-carboxylate | HCID 10563690 | 77% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07009056B2 |
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| Source dataset | uspto-grants-2006_03 |
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| ORD ID | ord-e5b65c6b4f0b4d19a6c74b200757b4c1 |
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| Source note | uspto-grants-2006_03 |
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