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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212526Generated: October 26, 2026

Water → 5-(Benzyloxy)-2,3-dihydro-1H-indole

https://huagongshe.com/reaction/2212526

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant5-BenzyloxyindoleHCID 14624—
ReactantPotassium HydroxideHCID 14797—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventAcetic AcidHCID 176—
Product5-(Benzyloxy)-2,3-dihydro-1H-indoleHCID 1679488189.2%

Reaction Steps

In analogy to the method described by Gordon W. Gribble, Joseph H. Hoffmann Synthesis 1977, 859–860, the following reaction was performed. To a precooled solution of 22.3 g (0.1 mol) 5-benzyloxyindole in 270 ml acetic acid, 19 g (0.3 mol) NaCNBH3 were added. The solution was stirred at RT for 2 h, the volume was reduced to one third and poured into 300 ml water. KOH was added under cooling and the solution was extracted with ether. The combined organic phases were washed with water, dried over Na2SO4 and evaporated to yield 20.1 g (89%) 5-Benzyloxy-2,3-dihydro-1H-indole as colorless oil, MS: 225 (M).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07102007B2
Source datasetuspto-grants-2006_09
ORD IDord-5ad8b4954ea04fea972d9a3833a3baff
Source noteuspto-grants-2006_09