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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2052687Generated: October 30, 2026

Indoline → 1-(2-Nitrophenyl)indoline

https://huagongshe.com/reaction/2052687

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndolineHCID 10328—
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
Product1-(2-Nitrophenyl)indolineHCID 7410518—

Reaction Conditions

Temperature120 °C

Reaction Steps

11.0 g (0.10 mole) of indoline and 28.2 g of 1-fluoro-2-nitrobenzene are combined and the resultant solution is stirred and heated to 120° C. and kept at that temperature 18 hours. The reaction mixture is then cooled to room temperature and partitioned between chloroform and water. The chloroform layer is separated, washed with water, dried and concentrated in vacuum. The residue is dissolved in isopropylether from which 1-(2-nitrophenyl)indoline, m.p. 62°-64° C., precipitates on standing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04186199
Source datasetuspto-grants-1980_01
ORD IDord-7f61eed643c049daa497e4313c3a42d2
Source noteuspto-grants-1980_01