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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248777Generated: November 1, 2026

Sodium borohydride → Methyl 4-[5-(2-hydroxyethyl)-1-propylindol-3-ylmethyl]-3-methoxybenzoate

https://huagongshe.com/reaction/2248777

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantMethyl 4-[5-(formylmethyl)-1-propylindol-3-ylmethyl]-3-methoxybenzoateHCID 19994986—
SolventMethanolHCID 887—
ProductMethyl 4-[5-(2-hydroxyethyl)-1-propylindol-3-ylmethyl]-3-methoxybenzoateHCID 1999499665%

Reaction Steps

Sodium borohydride (0.027 g) was added to a stirred solution of methyl 4-[5-(formylmethyl)-1-propylindol-3-ylmethyl]-3-methoxybenzoate (0.54 g) in methanol (15 ml) under a nitrogen atmosphere. After 30 min, the solvent was evaporated. The residue was dissolved in ethyl acetate, washed with water (twice), brine, and then dried (MgSO4) and evaporated. The product was purified by flash chromatography, eluting with 7:3 hexane:ethyl acetate, to give methyl 4-[5-(2-hydroxyethyl)-1-propylindol-3-ylmethyl]-3-methoxybenzoate (0.35 g, 65%) as an oil: partial NMR (300 MHz, DMSO-d6): 0.80(t, 3H, CH3), 1.70(m, 2H, CH2), 2.74(t, 2H, CH2), 3.56(t, 2H, CH2), 3.83(s, 3H, OCH3), 3.91(s, 3H, OCH3), 4.03(m, 4H, NCH2, ArCH2Ar').

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05041460
Source datasetuspto-grants-1991_08
ORD IDord-8340c86303114426909084b842b00ec9
Source noteuspto-grants-1991_08