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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615257Generated: November 3, 2026

1H-Indazole-6-carbaldehyde → 1-(1H-Indazol-6-yl)ethanol

https://huagongshe.com/reaction/1615257

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Indazole-6-carbaldehydeHCID 18538368—
ReactantHCID 178418573HCID 178418573—
SolventTetrahydrofuranHCID 8028—
Product1-(1H-Indazol-6-yl)ethanolHCID 6876114560.8%

Reaction Steps

To a solution of 1H-indazole-6-carbaldehyde (200 mg, 1.37 mmol) in THF (7 mL) at −78° C. was added methyl magnesium bromide (1.4 mL, 4.11 mmol) dropwise under argon. The solution was warmed to rt and quenched with saturated ammonium chloride (2 mL). The mixture was extracted into ethyl acetate (3×10 mL), dried over MgSO4 and concentrated. The yellow oil was purified by silica gel chromatography (EtOAc/Hex 4:1) to yield the title compound as a clear oil (135 mg, 60%). 1H NMR (400 MHz, CDCl3) δ 8.07 (s, 1H), 7.76 (s, 1H), 7.50-7.47 (m, 2H), 5.05 (q, 1H, J=7.4 Hz), 1.57 (d, 3H, J=7.2 Hz); MS ESI [M+H]+, calcd for [C9H10N2O+H]+ 163.1; found m/z 163.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765748B2
Source datasetuspto-grants-2014_07
ORD IDord-e42229c745e2446bafb7cca923dee6ad
Source noteuspto-grants-2014_07