Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651608Generated: November 1, 2026

Indene → HCID 14126784, compound

https://huagongshe.com/reaction/1651608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndeneHCID 7219—
ReactantPyrrolidineHCID 31268—
ReactantIndene oxideHCID 92838—
ProductHCID 14126784HCID 14126784—

Reaction Steps

1,2-Epoxy-2,3-dihydro-1-H indene, prepared from indene (34.2 g) according to the procedure of M. Imuta and H. Ziffer, J. Org. Chem., 44, 1351 (1979), was treated immediately with pyrrolidine (50 ml). The exothermic reaction mixture was set aside for 15 minutes and then evaporated to remove the excess pyrrolidine under reduced pressure. The residue was distilled under vacuum to yield trans-2,3-dihydro-2-hydroxy-1-(pyrrolidin-1-yl)-1H-indene (10.2 g), b.p. 148°-150°/0.25 torr.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04929627
Source datasetuspto-grants-1990_05
ORD IDord-b3ce0e97895b4295afb145d6c29c7ab8
Source noteuspto-grants-1990_05