Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1533989Generated: November 2, 2026

1-Methyl-1H-indole-4-carbaldehyde → alpha-(2-methoxyphenyl)-1-methyl-1H-indol-4-methanol

https://huagongshe.com/reaction/1533989

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Methyl-1H-indole-4-carbaldehydeHCID 17221111—
Reactant2-Bromo anisole magnesiumHCID 66862467—
SolventTetrahydrofuranHCID 8028—
Productalpha-(2-methoxyphenyl)-1-methyl-1H-indol-4-methanolHCID 19800111—

Reaction Steps

Using the procedure of Step B of Example 1, 36.8 g of the product of Step A and 104 ml of a solution of 2-bromo anisole magnesium compound in tetrahydrofuran titrating 1.94N were reacted. Extraction was carried out with ethyl acetate and the extracts were washed with salt water and brought to dryness. The residue was chromatographed on silica (eluant: methylene chloride) to obtain 46.5 g of the expected product melting at 95° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05086070
Source datasetuspto-grants-1992_02
ORD IDord-d6d471eee1f34576a19414009b9c5325
Source noteuspto-grants-1992_02