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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1393667Generated: November 2, 2026

Hydrochloric Acid → 1-[(Acetyloxy)methyl]-1H-indole-3-carboxylic acid

https://huagongshe.com/reaction/1393667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
ReactantBromomethyl acetateHCID 68536—
ReactantIndole-3-Carboxylic AcidHCID 69867—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1-[(Acetyloxy)methyl]-1H-indole-3-carboxylic acidHCID 2309196761%

Reaction Conditions

Temperature0 °C

Reaction Steps

1H-Indole-3-carboxylic acid (400 mg) was dissolved in N,N-dimethylformamide (6 ml) and cooled to 0° C. Sodium hydride (500 mg) was added to the solution in two divided portions, and the mixture was stirred as such for 30 minutes. Bromomethyl acetate (0.32 ml) was added slowly dropwise thereto, and the mixture was stirred for 15 minutes at 0° C., warmed to room temperature and stirred for 45 minutes. The mixture was cooled to 0° C., and water was added to the mixture which was then acidified by 2 N hydrochloric acid and extracted with ethyl acetate. The extract was dried over sodium sulfate anhydrous and concentrated under reduced pressure. The residue was purified by column chromatography (eluting solvent; dichloromethane:methanol 50:1) to give the title compound (354 mg, Y.:61%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07345180B2
Source datasetuspto-grants-2008_03
ORD IDord-d184009954a14e19a2dd781002a6dc3c
Source noteuspto-grants-2008_03