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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195899Generated: October 25, 2026

Sodium Hydroxide → 1-(5-Methoxy-2-methyl-1H-indol-3-yl)ethanone

https://huagongshe.com/reaction/1195899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantDimethylacetamideHCID 31374—
ReactantMethoxy-2-methylindoleHCID 53764995—
SolventWaterHCID 962—
Product1-(5-Methoxy-2-methyl-1H-indol-3-yl)ethanoneHCID 60482367.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

Dimethylacetamide (17.5 ml, 188.4 mmol) is added dropwise with stirring to phosphorous oxychloride (12.9 ml, 138.2 mmol) at 0° C. Stirring is maintained for 45 minutes, at which time the bath is removed and -methoxy-2-methylindole (20.25 g, 125.6 mmol) in 15 ml of dimethylacetamide is added dropwise over a period of 75 minutes. The resulting mixture is warmed to 40°-45° C. for 4 hours. The reaction mixture is cooled to 0° C, and 100 g of ice water is added followed by dropwise addition of a solution of sodium hydroxide (50 g) in water (75 ml). The first 1/3 of this sodium hydroxide solution is added slowly and the remainder is added quickly. The exothermic reaction is quickly warmed to boiling for 15 minutes, cooled to room temperature and refrigerated overnight. The resulting crystals are collected by filtration and rinsed four times with water. Recrystallization from ethanol/water gives 17.2 g (67.2%) of pure 1-(5-methoxy-2-methyl-1H-indol-3- yl)ethanone; mp 229.0°-230.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05112846
Source datasetuspto-grants-1992_05
ORD IDord-71850abaab6c45a6bc4cd6f38c03d618
Source noteuspto-grants-1992_05