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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73937Generated: October 26, 2026

Ethyl iodoacetate → (6-Amino-1H-indol-3-yl)-acetic acid ethyl ester

https://huagongshe.com/reaction/73937

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl iodoacetateHCID 12183—
Reactant6-Nitro-1H-indoleHCID 78502—
SolventAcetonitrileHCID 6342—
Product(6-Amino-1H-indol-3-yl)-acetic acid ethyl esterHCID 66675483—

Reaction Steps

(6-Amino-1H-indol-3-yl)-acetic acid ethyl ester (B-17) was synthesized following the general scheme above starting from 6-nitroindole and iodo-acetic acid ethyl ester. Overall yield (24%). HPLC ret. time 0.95 min, 10-99% CH3CN, 5 min run; ESI-MS 219.2 m/z (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829204B2
Source datasetuspto-grants-2014_09
ORD IDord-ed116ac2db13497eaec502a4321fada4
Source noteuspto-grants-2014_09