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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 913796Generated: October 27, 2026

Sodium borohydride → (7-Methyl-2-((2-(trimethylsilyl)ethoxy)methyl)-2H-indazol-5-yl)methanol

https://huagongshe.com/reaction/913796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant7-Methyl-2-((2-(trimethylsilyl)ethoxy)methyl)-2H-indazole-5-carbaldehydeHCID 11572862—
SolventEthanolHCID 702—
Product(7-Methyl-2-((2-(trimethylsilyl)ethoxy)methyl)-2H-indazol-5-yl)methanolHCID 57545931—

Reaction Steps

To a solution of 7-methyl-2-((2-(trimethylsilyl)ethoxy)methyl)-2H-indazole-5-carbaldehyde (150 mg, 0.516 mmol) in ethanol (4 mL) at room temperature was added sodium borohydride (19.5 mg, 0.516 mmol). The reaction was stirred at room temperature for 20 min, cooled to 0° C., and quenched by the cautious addition of saturated ammonium chloride. The reaction was poured into diethyl ether and washed with water (2×), then brine, dried over magnesium sulfate, and concentrated to give 139 mg (92%) as an oil. 1H-NMR (CDCl3, 500 MHz) δ 7.97 (s, 1H), 7.38 (s, 1H), 7.01 (s, 1H), 5.65 (s, 2H), 4.64 (s, 2H), 3.58 (m, 2H), 2.57 (s, 3H), 2.51 (bs, 1H), 0.89 (m, 2H), −0.07 (s, 9H); 13C NMR (126 MHz, CDCl3) δ ppm 148.9, 135.1, 128.2, 125.5, 122.9, 121.7, 115.4, 81.5, 67.2, 65.6, 17.7, 17.1, −1.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026257B2
Source datasetuspto-grants-2011_09
ORD IDord-f6651d761e424ed4a835279a3af694c2
Source noteuspto-grants-2011_09