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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1824942Generated: November 2, 2026

Isopropenyl acetate → 286836-32-6

https://huagongshe.com/reaction/1824942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropenyl acetateHCID 7916—
ReactantBenzofuran, 5-bromo-HCID 90015—
ReactantMethoxytri-n-butylstannaneHCID 11964040—
CatalystPalladium ChlorideHCID 24290—
CatalystTri-o-tolylphosphineHCID 80271—
SolventTolueneHCID 1140—
Product286836-32-6HCID 22144718103.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 1.90 gm (10 mmol) 5-bromobenzofuran, 183 mg (0.6 mmol) tri(o-tolyl)phosphine, 4.3 mL (15 mMol) tributyl tin methoxide, and 1.7 mL (15.4 mMol) isopropenyl acetate in 55 mL toluene was sparged with nitrogen for 15 minutes. To this mixture were then added 54 mg (0.3 mMol) palladium(II) chloride and the mixture was heated to 100° C. for 3 hours. The reaction mixture was cooled to room temperature and concentrated under reduced pressure. The residue was filtered through a bed of 100 gm silica gel, eluting with 1 liter of 1:1 hexane:ethyl acetate. Fractions containing crude product were combined and concentrated under reduced pressure. The residue was subjected to silica gel chromatography, eluting with a gradient of hexane containing from 0–20% ethyl acetate. Fractions containing product were combined and concentrated under reduced pressure to provide about 1.8 gm of the desired compound as an oil which gradually crystallized.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07045545B1
Source datasetuspto-grants-2006_05
ORD IDord-fbc6a9d603e34bc796009c5a7363e8c4
Source noteuspto-grants-2006_05