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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1031490Generated: November 1, 2026

Indole-3-Acetic Acid → Indole-3-propanol

https://huagongshe.com/reaction/1031490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndole-3-Acetic AcidHCID 802—
ReactantWaterHCID 962—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantAluminium lithium hydrideHCID 21226445—
ProductIndole-3-propanolHCID 7711580%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred suspension of LiAlH4 (3.24g) in THF (200 mL) at 0° C. and under N2 atmosphere was added tropwise a THF solution (50 mL) containing indole-3-acetic acid (10.0 g). After the addition was complete, the reaction was heated at reflux for 3 h, after which time the mixture was cooled to 0° C. and water (3.3 mL) added, followed by 15% NaOH (3.3 mL), and finally additional water (9.9 mL). The reaction was filtered and the filter cake washed with Et2O. The organic layers were combined, dried with anhydrous MgSO4, filtered, and concentrated under reduced pressure to yield 3-(2hydroxyethyl)indole (VI; 7.4 g; 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04954502
Source datasetuspto-grants-1990_09
ORD IDord-84e9385837e842b682f10d75692ccbdd
Source noteuspto-grants-1990_09