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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1517323Generated: November 4, 2026

Ethanol → HCID 68560618, compound

https://huagongshe.com/reaction/1517323

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantIsobutyl iodideHCID 10556—
ReactantSodium sulfide nonahydrateHCID 73972—
ReactantHCID 10511487HCID 10511487—
SolventWaterHCID 962—
ProductHCID 68560618HCID 6856061841%

Reaction Conditions

Temperature50 °C

Reaction Steps

An ethanol (14 mL) solution of indolin-5-yl thiocyanate (compound described in the document J. Med. Chem., 1998, vol. 41, p. 1598; 1.33 g, 7.55 mmol) was added to a solution of sodium sulfide nonahydrate (1.84 g, 7.66 mmol) in water (2.8 mL), and the mixture was stirred at 50° C. for 2 hours. To the reaction solution, an ethanol (2.4 mL) solution of isobutyl iodide (1.2 mL, 10.4 mmol) was added, and the mixture was stirred at 50° C. for 2 hours. To the reaction solution, water was added, followed by extraction with ether three times. The obtained organic layer was washed with saturated saline and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate=90:10-80:20-55:45, V/V) to obtain the title compound as brown oil (0.65 g, yield: 41%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08232287B2
Source datasetuspto-grants-2012_07
ORD IDord-6164950c4d3f48f4aa1a2398d9f824f6
Source noteuspto-grants-2012_07