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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51465Generated: October 27, 2026

Benzenepropanal → 3-Phenylmethyl-7-methoxyindole

https://huagongshe.com/reaction/51465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenepropanalHCID 7707—
ReactantPhosphorus trichlorideHCID 24387—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Methoxyphenylhydrazine HydrochlorideHCID 2849445—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product3-Phenylmethyl-7-methoxyindoleHCID 22740738—

Reaction Steps

A mixture of 15 gm (0.086 mol) of 2-methoxyphenylhydrazine hydrochloride and 12 mL (0.09 mol) of 3-phenylpropionaldehyde in 300 mL of toluene was refluxed for 1.5 hours with azeotropic removal of water. The suspension was cooled, evaporated in vacuo and the residue dissolved in 500 mL of dichloromethane and stirred with 9 mL (0.09 mol) of phosphorous trichloride for 18 hours. The solution was poured into ice-water, stirred well, and made basic with sodium bicarbonate. The organic phase was washed with saturated sodium chloride, dried over sodium sulfate, and evaporated in vacuo. The residue was chromatographed on silica gel eluting with a gradient hexane/5-15% ethyl ether to give product, 8.0 gm, 40%, as a viscous oil. 1H NMR (CDCl3) δ: 3.95 (s, 3H), 4.10 (s, 2H), 6.65 (d, 1H), 6.90 (s, 1H), 7.00 (t, 1H), 7.10 (d, 1H), 7.20 (m, 1H), 7.30 (m, 4H), 8.20 (br s, 1H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713645B1
Source datasetuspto-grants-2004_03
ORD IDord-e5b31f1a44974878a00a6afaac8c47d2
Source noteuspto-grants-2004_03