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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655062Generated: November 2, 2026

Indole → methyl 2-(1H-indol-1-yl)acetate

https://huagongshe.com/reaction/1655062

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
ReactantMethyl bromoacetateHCID 60984—
Productmethyl 2-(1H-indol-1-yl)acetateHCID 966836—

Reaction Steps

This compound was prepared from indole and methyl bromoacetate by the method described in Example 10, part i. The reaction mixture was worked up by concentrating in vacuo, diluting with water and extracting with ethyl acetate (3x). The combined extracts were washed with water (3x) and brine, dried and evaporated to an oil. The residue was purified by chromatography on flash silica eluting with petroleum spirit 40°-60° C.--diethyl ether (5:1, 2:1) to give the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05410061
Source datasetuspto-grants-1995_04
ORD IDord-ae578bbd2dcd4899a9911b36c06ae63a
Source noteuspto-grants-1995_04