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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4928Generated: October 23, 2026

Hydrochloric Acid → N-acetyl-5-bromo-7-cyanoindoline

https://huagongshe.com/en/reaction/4928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium CyanideHCID 8929—
ReactantSodium CarbonateHCID 10340—
Reactant1-(7-Amino-5-bromoindolin-1-yl)ethanoneHCID 19711338—
ReactantSodium NitriteHCID 23668193—
SolventHCID 178418260HCID 178418260—
ProductN-acetyl-5-bromo-7-cyanoindolineHCID 1979720881.1%

Reaction Conditions

Temperature-1 °C

Reaction Steps

Into 6N hydrochloric acid (178.5 ml) was suspended N-acetyl-7-amino-5-bromoindoline (51.0 g), and aqueous solution (212 ml) of sodium nitrite (21.2 g) was dropwise added thereto under cooling with stirring over 30 minutes and at the inside temperature of not higher than -1° C. After stirred for 30 minutes at the temperature as such, sodium carbonate was added to the reaction mixture to neutralize it. This reaction mixture was poured into aqueous solution (200 ml) of copper cyanide (27.5 g) and sodium cyanide (30.7 g), and the mixture was allowed to stand for one night at room temperature. The reaction mixture was again subjected to stirring for 30 minutes at the inside temperature of 50° C. and was cooled to give a deposited crystal, which was then collected by filtration, washed with water and dried. The crude crystal was recrystallized from acetonitrile to give the intended compound 43.0 g (81.1%). M.P.: 170°-175° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05242912
Source datasetuspto-grants-1993_09
ORD IDord-45f32967a0dc4124843cfe2d5c8768c7
Source noteuspto-grants-1993_09