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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485346Generated: October 29, 2026

Dimethyl Sulfoxide → 3-(6-carboxyhex-1-enyl)-N-(3-pyridyl)indole

https://huagongshe.com/reaction/485346

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
Reactant(5-Carboxypentyl)triphenylphosphanium bromideHCID 2779280—
ReactantHCID 13490349HCID 13490349—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
Product3-(6-carboxyhex-1-enyl)-N-(3-pyridyl)indoleHCID 54158455—

Reaction Steps

A solution of dimsyllithium (from 80 ml of dimethylsulfoxide and 13 ml of 2.1M n-butyllithium) is stirred under nitrogen at room temperature, and 6.2 g of 5-carboxypentyltriphenylphosphonium bromide is added in portions. The reaction mixture is stirred for 30 minutes and 3.0 g of N-(3-pyridyl)indole-3-carboxaldehyde is added. After 18 hours at room temperature, the reaction mixture is diluted with 240 ml of water and extracted with 100 ml of ethyl acetate. The aqueous phase is neutralized with 1.1 ml of concentrated hydrochloric acid and extracted with ethyl acetate. The extracts are dried over sodium sulfate and evaporated to an oil which is triturated with ether to give a semi-solid which is recrystallized from methanol to yield 3-(6-carboxyhex-1-enyl)-N-(3-pyridyl)indole, m.p. 124°-125°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04536505
Source datasetuspto-grants-1985_08
ORD IDord-2dc8df6ce6464c01b10bdb1e35513d3e
Source noteuspto-grants-1985_08