HuagongsheHuagongshe Chemistry Print Report · For research reference only
Indene → HCID 14126784, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Indene | HCID 7219 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | Indene oxide | HCID 92838 | — |
| Product | HCID 14126784 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05010085 |
| Source dataset | uspto-grants-1991_04 |
| ORD ID | ord-69aef65087fc4fbb841f62084f0cb8ed |
| Source note | uspto-grants-1991_04 |