Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2217080Generated: October 30, 2026

Indole → 1-Aminoindole

https://huagongshe.com/reaction/2217080

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
Reactanthydroxylamine-O-sulfonic acidHCID 76284—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 86597979HCID 86597979—
ReactantHOSA indole NMPHCID 131725955—
CatalystHCID 86597979HCID 86597979—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product1-AminoindoleHCID 64322190.2%

Reaction Steps

A solution of 33.8 kg (32.8 kg corrected for 97% purity) of hydroxylamine-O-sulfonic acid (HOSA) and 15.8 kg (15.6 kg corrected for 99% purity) of indole in 120.2 kg of N-methylpyrrolidinone (NMP), is prepared and chilled to 0–5° C. A second solution is prepared from 67.0 kg (63.7 kg corrected for 95% purity) of potassium tert-butoxide and 122.6 kg of NMP. An amination vessel is charged with 47.0 kg of NMP and an initial charge of 2.2 kg of the potassium tert-butoxide/NMP solution. The HOSA/indole/NMP solution and the remaining potassium tert-butoxide/NMP solution are then simultaneously and proportionally metered using a metering pumping system consisting of a dual head plunger pump together with coriolis mass flow meters into the amination vessel over a period of 185 minutes while maintaining a reaction temperature of 20–30° C. to yield a solution containing 15.9 kg (90.2% yield) of 1H-indol-1-amine as determined by external standard HPLC assay.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07112682B2
Source datasetuspto-grants-2006_09
ORD IDord-8f03ef23ba7d46769b959d62f3548a9d
Source noteuspto-grants-2006_09