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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726424Generated: November 1, 2026

5-Methoxyindole-3-carbaldehyde → (5-methoxy-1H-indol-3-yl)methanol

https://huagongshe.com/reaction/1726424

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Methoxyindole-3-carbaldehydeHCID 82758—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventPotassium CarbonateHCID 11430—
Product(5-methoxy-1H-indol-3-yl)methanolHCID 425529370%

Reaction Steps

To a solution of sodium borohydride (2 grams, 0.05 mol) in methanol (15 ml), a solution of 5-methoxy-1H-indol-3-carboxaldehyde 2 (1 gram, 0.006 mol) dissolved in THF (20 ml) and methanol (15 ml) were combined and stirred at ambient temperature for 16 hours. The reaction was diluted with water and potassium carbonate (to saturation) and stirred to quench unreacted sodium borohydride. Diethyl ether was used to extract the product from the quenched solution. Following layers separation, the aqueous layer was further extracted (2×) with diethyl ether. The combined organic pats were dried over sodium sulfate and evaporated to dryness to yield a light colored solid 141 (736 mg, 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491831B2
Source datasetuspto-grants-2009_02
ORD IDord-121b0cddc645495fbba2a9bade33101c
Source noteuspto-grants-2009_02