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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085482Generated: October 30, 2026

Indene → HCID 14126784, compound

https://huagongshe.com/reaction/1085482

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 numberUS05010085
Source datasetuspto-grants-1991_04
ORD IDord-69aef65087fc4fbb841f62084f0cb8ed
Source noteuspto-grants-1991_04