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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108476Generated: October 31, 2026

1-benzyl-2,3-dihydroindole-5-carbaldehyde → 5-Methylindoline

https://huagongshe.com/reaction/1108476

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-benzyl-2,3-dihydroindole-5-carbaldehydeHCID 927567—
ReactantHCID 178418361HCID 178418361—
SolventEthanolHCID 702—
Product5-MethylindolineHCID 1402367985%

Reaction Steps

Into a 200 mλ pressure resistant reactor (autoclave) equipped with a stirrer, 20 g (0.084 mol) of 1-benzyl-5-formylindoline and 100 mλ of ethanol were charged, and the interior of the reactor was flushed with nitrogen. 2 g of 10% Pd/C was introduced, and the reactor was closed, whereupon hydrogen was introduced from a hydrogen supply pipe and reacted at 80° C. for 6 hours while adjusting the initial pressure of hydrogen in the reactor to be 6 2 kg/cm. Upon confirming the ceasing of absorption of hydrogen, the reaction was terminated. Then, the reaction solution was cooled to room temperature, and the hydrogen was released, and the palladium catalyst (10% Pd/C) was collected by filtration, and ethanol was distilled off under reduced pressure to obtain a colorless liquid as the residue. The obtained liquid was subjected to vacuum distillation to obtain 9.5 g of 5-methylindoline having a boiling point of from 56 to 57° C./0.3 mmHg. The yield was 85% (based on 1-benzyl-5-formylindoline).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06066744
Source datasetuspto-grants-2000_05
ORD IDord-7efaae340d6b472aaadce8a2753236ad
Source noteuspto-grants-2000_05