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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355166Generated: October 28, 2026

1H-Indole, 1-ethyl-2-methyl- → HCID 20442778, compound

https://huagongshe.com/reaction/355166

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Indole, 1-ethyl-2-methyl-HCID 170432—
ReactantHCID 54180223HCID 54180223—
SolventAcetic AnhydrideHCID 7918—
ProductHCID 20442778HCID 20442778—

Reaction Steps

A mixture of 7.0 g (0.02 mole) of 4-(2-phenyl-3-indolyl)-2,3-dichloro-4-oxo-2-butenoic acid (prepared in part A above), 3.5 g (0.02 mole) of 1-ethyl-2-methylindole and 200 ml of acetic anhydride was stirred at ambient temperature in an atmosphere of air for approximately seventeen hours. The pale blue solid that formed was collected by filtration and dried in vacuo at 60° C. to obtain 5-(2-phenyl-3-indolyl)-5-(1-ethyl-2-methyl-3-indolyl)-3,4-dichloro-2(5H)-furanone (Formula V: R=Y=Y1 =H; R1 =C6H5 ; R2 =CH3CH2 ; R3 =CH3) as a tan-colored solid which started to sinter at 213° C. and was completely melted at 225° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04377698
Source datasetuspto-grants-1983_03
ORD IDord-e0540021c070425bb766d79316ae2e46
Source noteuspto-grants-1983_03