Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 975145Generated: October 25, 2026

5-(3-Hydroxy-1-but-1-enyl)-3-(N-methyl-4-piperidyl)-1H-indole → 5-(3-Hydroxy-1-butyl)-3-(N-methyl-4-piperidyl)-1H-indole

https://huagongshe.com/reaction/975145

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(3-Hydroxy-1-but-1-enyl)-3-(N-methyl-4-piperidyl)-1H-indoleHCID 54086563—
CatalystPalladiumHCID 23938—
SolventDichloromethaneHCID 6344—
Product5-(3-Hydroxy-1-butyl)-3-(N-methyl-4-piperidyl)-1H-indoleHCID 19970945—

Reaction Steps

Obtained from the title compound of Example 42 by a procedure similar to that described in Example 2, but using 10% palladium on charcoal as catalyst, as a foam. Rf 0.50 (SS 4). C,73.39; H,8.77; N,9.06. C18H26N2O; 0.125 CH2Cl2 requires C,73.28; H,8.91; N,9.43%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05607960
Source datasetuspto-grants-1997_03
ORD IDord-631587a7f2de4c9a86ff6b175d215833
Source noteuspto-grants-1997_03