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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1636063Generated: October 30, 2026

Potassium Carbonate → N-Amino-3-chloro-1H-indole

https://huagongshe.com/reaction/1636063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPotassium HydroxideHCID 14797—
Reactanthydroxylamine-O-sulfonic acidHCID 76284—
Reactant3-Chloro-1H-indoleHCID 177790—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
ProductN-Amino-3-chloro-1H-indoleHCID 996419892.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 12 L round bottom flask equipped with a mechanical stirrer, thermometer and a Gooch tube was added sieve-dried dimethylformamide (2.8 L), 3-chloroindole (240 g, 91.6% pure), milled potassium carbonate (200.4 g), milled potassium hydroxide (574.3 g, 85% pure) and dimethylformamide (900 mL) at −2° to 5° C. The reaction mixture was cooled to about 0° C. and hydroxylamine-O-sulfonic acid (338.2 g, 97% pure) was added portionwise via the Gooch tube over a period of about 4 hrs, maintaining the reaction temperature at about 0° C. When the reaction was >95% complete (by high performance liquid chromatography), the reaction mixture was poured into a well-stirred, cold mixture of water (18 L and 3.6 kg ice) and toluene (2.4 L). After about 5 mins, the phases were separated and the aqueous phase was extracted with toluene (1×2.4 L and 1×1 L). The organic fractions were combined and filtered through Celite. The filtrate was concentrated under reduced pressure (about 50 mm Hg) at about 60° C. to yield 245 g (86%) of product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06512125B1
Source datasetuspto-grants-2003_01
ORD IDord-dcdb0d9fe2b2467abf27c436edabac20
Source noteuspto-grants-2003_01