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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908533Generated: October 27, 2026

Water → 2-(5-nitro-1H-indol-2-yl)propan-1-ol

https://huagongshe.com/reaction/1908533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantAluminium lithium hydrideHCID 21226445—
Reactantethyl 2-(5-nitro-1H-indol-2-yl)propanoateHCID 59129193—
SolventTetrahydrofuranHCID 8028—
Product2-(5-nitro-1H-indol-2-yl)propan-1-olHCID 5912939283.6%

Reaction Steps

To a cooled solution of LiAlH4 (1.0 M in THF, 1.2 mL, 1.2 mmol) in THF (5.3 mL) at 0° C. was added a solution of ethyl 2-(5-nitro-1H-indol-2-yl)propanoate (0.20 g, 0.76 mmol) in THF (3.66 mL) dropwise. After addition, the mixture was allowed to warm up to room temperature and was stirred at room temperature for 3 h. The mixture was cooled to 0° C. Water (2 mL) was slowly added followed by careful addition of 15% NaOH (2 mL) and water (4 mL). The mixture was stirred at room temperature for 0.5 h and was then filtered through a short plug of celite using ethyl acetate. The organic layer was separated from the aqueous layer, dried over Na2SO4, filtered and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel (ethyl acetate/hexane=1/1) to give 2-(5-nitro-1H-indol-2-yl)propan-1-ol (0.14 g, 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598181B2
Source datasetuspto-grants-2013_12
ORD IDord-4dcdf99be7b141d19d3bf30049531acc
Source noteuspto-grants-2013_12