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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252571Generated: October 26, 2026

Ethanol → 6-Iodoindoline

https://huagongshe.com/reaction/252571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
Reactant1-Acetyl-6-iodoindolineHCID 11666396—
SolventWaterHCID 962—
Product6-IodoindolineHCID 1161569664%

Reaction Steps

1-Acetyl-6-iodoindoline (1.06 g, 3.7 mmol), NaOH (1.16 g, 29 mmol), EtOH (8 mL), and H2O (6 mL) are heated at 90° C. overnight. The reaction mixture is then partitioned between H2O and EtOAc. The organic layer is extracted into aqueous HCl. The aqueous layer is in turn basified with NaOH, and is extracted with EtOAc. The organic layer is dried and concentrated. Hexane trituration yields 6-iodoindoline (577 mg, 64%) as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868037B2
Source datasetuspto-grants-2011_01
ORD IDord-a0f13259a14d43c5b16fbd2049ae4af8
Source noteuspto-grants-2011_01