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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249618Generated: November 2, 2026

Toluene → HCID 13340174, compound

https://huagongshe.com/reaction/1249618

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium HydroxideHCID 14798—
Reactant2-Phenyl-2H,4H-[1,3]dioxino[5,4-b]pyridine-6-carbaldehydeHCID 13748401—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventWaterHCID 962—
ProductHCID 13340174HCID 13340174—

Reaction Steps

In a two liter 3-neck, round bottom flask, fitted with a mechanical stirrer, a thermometer and a reflux condenser, a heterogeneous mixture of 2-phenyl-4H-1,3-dioxino[5,4-b]pyridine-6-carbaldehyde (24.1 g., 0.1 mole) sodium hydroxide (24.0 g., 0.6 mole) and methyltriphenylphosphonium bromide (71.5 g., 0.2 mole) in toluene (200 ml.) and water (600 ml.) was stirred at room temperature for 24 hours. The toluene layer was separated and the aqueous layer was washed with toluene (100 ml.). The combined toluene layers were dried over anhydrous magnesium sulfate. The toluene solution was then passed through a 10 mm. pad of silica gel which was then washed with 1 liter of ether/hexane solution (v/v 3:2). Evaporation of the solvents on a rotary evaporation in vacuo gave the crystalline 2-phenyl-6-vinyl-4H-1,3-dioxino[5,4-b]pyridine, 14.3 g. (59%); m.p. 54°-57° C.; mass spec (70 eV) m/e 211 (M+), 134, 133, 132, 106, 105, 104.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04632992
Source datasetuspto-grants-1986_12
ORD IDord-b901cae111e9427e8a6b1fd7d2db39c5
Source noteuspto-grants-1986_12