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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029709Generated: October 30, 2026

Water → 5-(Benzyloxy)-1H-indol-1-amine

https://huagongshe.com/reaction/1029709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant5-BenzyloxyindoleHCID 14624—
ReactantPotassium HydroxideHCID 14797—
Reactanthydroxylamine-O-sulfonic acidHCID 76284—
SolventDimethylformamideHCID 6228—
Product5-(Benzyloxy)-1H-indol-1-amineHCID 14988297133.1%

Reaction Steps

To 5-phenylmethoxyindole (50 g) in 300 ml of dimethylformamide at ice bath temperature was added milled potassium hydroxide (62.72 g). Then hydroxylamine-O-sulfonic acid (32.93 g) was added portionwise, keeping the internal temperature below 20° C. After the addition was complete, the mixture was stirred for one hour, then poured into water and extracted with ethyl acetate. The organic layer was washed with water and dried (sat. NaCl, anhy. MgSO4). After filtration, the solvent was evaporated to yield an oil (71 g), which was eluted with dichloromethane on silica gel columns via HPLC. The desired fractions were concentrated to yield a solid (21.15 g). Of this material, 3.0 g was triturated with ether to yield a solid, 2.4 g, m.p. 126°-128° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05102891
Source datasetuspto-grants-1992_04
ORD IDord-4075b2b1b94d4663b32819e722d4f79a
Source noteuspto-grants-1992_04