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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1704652Generated: October 29, 2026

Indene → 2-[2-(1H-inden-3-yl)ethyl]pyridine

https://huagongshe.com/reaction/1704652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndeneHCID 7219—
Reactant2-VinylpyridineHCID 7521—
ReactantPotassium tert-butoxideHCID 23665647—
SolventAcetic AcidHCID 176—
Product2-[2-(1H-inden-3-yl)ethyl]pyridineHCID 12135562—

Reaction Steps

This compound is prepared as described by Dressler and Kurland J.O.C. 29, 175 (1964). Under nitrogen gas, 500 g. indene plus 5 g. potassium t-butoxide are stirred and heated to 130°. 2-Vinyl pyridine (220 g., 2.0 M) is added dropwise over a period of 1 hour keeping the temperature at 135°-145° C. during addition and for 2 hours after addition is completed. The reaction mixture is cooled and 25 ml. acetic acid is added, followed by filtration. A flash distillation yields 395 g. (84%) crude product boiling 160°-175°/0.3 mm. This is redistilled to give 353 g. (75%) of oil (3-[2[(pyridyl)ethyl]indene) boiling point 135°-140°/0.1 mm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04127578
Source datasetuspto-grants-1978_11
ORD IDord-be8c321db5d349beba33abd044d00579
Source noteuspto-grants-1978_11