Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47240Generated: October 26, 2026

Formaldehyde → 1-Butylaminomethyl-3-(1H-pyrrol-2-ylmethylene)-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/47240

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantButylamineHCID 8007—
ReactantHexaneHCID 8058—
Reactant(Z)-3-((1H-pyrrol-2-yl)methylene)indolin-2-oneHCID 5908088—
SolventEthanolHCID 702—
Product1-Butylaminomethyl-3-(1H-pyrrol-2-ylmethylene)-1,3-dihydro-indol-2-oneHCID 68834641—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of Z-(1H-Pyrrol-2-ylmethylene)-1,3-dihydro-indol-2-one (120.0 mg, 0.571 mmol), paraformaldehyde (17.1 mg, 0.571 mmol), and butylamine (56.4 μL, 0.571 mmol) in 5.5 mL of EtOH was heated at reflux for 2.5 h. Then reaction mixture was treated with 2 mL of hexane was and then cooled to 0° C. The reaction mixture was then filtered to remove Z-(1H-Pyrrol-2-ylmethylene)-1,3-dihydro-indol-2-one. The filtrate was partitioned between dilute HCl and ethyl acetate. The organic layer was removed and the aqueous layer washed with 15 mL Ethyl acetate. The aqueous phase was made basic to pH 8 with saturated NaHCO3 and extracted with ethyl acetate. The ethyl acetate layer was washed with H2O, brine and dried over anhydrous Na2SO4. The solvent was removed in vacuo to give 58 mg of yellow oil. The oil was purified by chromatography (silica gel, 1:1/hexane:ethyl acetate) to give the title compound (51.6 mg, 31%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06699863B1
Source datasetuspto-grants-2004_03
ORD IDord-df79f2cf7a9b4263834f59cd3ebdf5e4
Source noteuspto-grants-2004_03