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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358915Generated: November 2, 2026

Water → HCID 21965165, compound

https://huagongshe.com/reaction/2358915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDibenzo(b,d)furan-2-carboxaldehydeHCID 220843—
ReactantButyllithiumHCID 178418339—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 21965165HCID 2196516595%

Reaction Conditions

Temperature0 °C

Reaction Steps

22.7 g (63.7 mmol) of Methyl triphenylphosphonium bromide and 200 ml of dry THF are placed in a dried 500 ml three necked round bottomed flask, equipped with a magnetic stirrer and the reaction mixture is cooled to 0° C. internal temperature with a NaCl/ice bath. 41.8 ml (66.9 mmol) of 1.6 M Butyl lithium solution in Hexane are added within 30 minutes while keeping the internal temperature below 3° C. The reaction mixture is stirred at the same temperature for 45 minutes, then 47.2 mmol of Dibenzofuran-2-carboxaldehyde dissolved in 100 ml of dry THF are added within 30 minutes. After two hours the reaction mixture is warmed to room temperature, added to 500 ml of water and extracted three times with 500 ml of Ethylacetate. The combined organic phases are washed once with 500 ml of a 1:1 mixture of buffer pH=1 and brine, once with 30 ml of brine, dried over Magnesiumsulfate, filtered and evaporated. The crude product is dissolved in Dichloromethane, 100 g of silica are added and the solvent is evaporated. The resulting powder is added on top of 300 g of silica in a sintered glass funnel and the product eluted with Hexane/Ethylacetate=8:1. The product is crystallized from 2-Propanol. 2-Vinyl-dibenzofuran is isolated in 95% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08685541B2
Source datasetuspto-grants-2014_04
ORD IDord-6c437c865f264842a4464ded9b704d09
Source noteuspto-grants-2014_04