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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250198Generated: October 26, 2026

4-Methoxy-1H-indole → 4-methoxy-2,3-dihydro-1H-indole

https://huagongshe.com/reaction/250198

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxy-1H-indoleHCID 138363—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventAcetic AcidHCID 176—
Product4-methoxy-2,3-dihydro-1H-indoleHCID 1624444154.2%

Reaction Steps

4-methoxyindole (0.735 g) was dissolved in acetic acid (25 ml) and cooled in an ice bath. To this solution was added sodium cyanoborohydride (0.942 g) in portions. After the addition was complete, the solution was allowed to come to room temperature and the solution was stirred for an hour. The solvent was removed under vacuum and the residue was taken up in ethyl acetate, washed with sodium carbonate solution, water and finally with brine. The organic layer was evaporated and the resulting product was purified on a silica gel column eluting with ethyl acetate:dichloromethane (5:95) to give 0.404 g of 4-methoxyindoline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863305B2
Source datasetuspto-grants-2011_01
ORD IDord-65321f0565a2421a96157812585bb734
Source noteuspto-grants-2011_01