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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422847Generated: November 2, 2026

Water → 2-Hydroxy-5-nitroindane

https://huagongshe.com/reaction/1422847

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant5-Nitro-2-indanoneHCID 1502066—
ReactantSodium borohydrideHCID 4311764—
SolventIsopropanol ethanolHCID 22179027—
Product2-Hydroxy-5-nitroindaneHCID 368592783.2%

Reaction Steps

5-nitro-2-indanone (5.3 g, 30 mmol) was dissolved in EtOH: i-PrOH (1:1, 150 mL). NaBH4 (1.7 g, 45 mmol) was added portion by portion at room temperature. The reaction mixture was stirred at r.t for additional 30 min and water was added at 0° C. (ice-water bath). The reaction mixture was extracted with EtOAc (100 mL×3) and the combined organic layers were washed with water and brine and dried over Na2SO4. Purification of the concentrated crude product by column chromatography (EtOAc:Hexane=4:6) afforded the title product as a pale yellow oil (4.47 g, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927548B2
Source datasetuspto-grants-2015_01
ORD IDord-4d9bd03370604442bfe5fe16b9383313
Source noteuspto-grants-2015_01