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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 7-Methyl-2-((2-(trimethylsilyl)ethoxy)methyl)-2H-indazole-5-carbaldehyde | HCID 11572862 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (7-Methyl-2-((2-(trimethylsilyl)ethoxy)methyl)-2H-indazol-5-yl)methanol | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08026257B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-f6651d761e424ed4a835279a3af694c2 |
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| Source note | uspto-grants-2011_09 |
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