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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1078695Generated: October 26, 2026

Benzaldehyde → 7-[(Trifluoromethylsulfonyl)oxy]-3-phenymethylene-benzopyran-4-one

https://huagongshe.com/reaction/1078695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantPyrrolidineHCID 31268—
Reactant7-Trifluoromethylsulfonyloxy-benzopyran-4-oneHCID 21955570—
SolventMethanolHCID 887—
Product7-[(Trifluoromethylsulfonyl)oxy]-3-phenymethylene-benzopyran-4-oneHCID 5387595875%

Reaction Steps

To a stirred solution of the product of Step C (27 g, 91.2 mmole) in 183 mL of methanol was added benzaldehyde (11.1 mL, 109 mmole) followed by pyrrolidine (9.1 mL, 109 mmole). The mixture was stirred at room temperature overnight, cooled to 0° C. and filtered. The solid was washed once with 50 mL of ice-cold methanol and then dried in vacuo; 35.2 g, (75% yield) of the title product was recovered.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05550152
Source datasetuspto-grants-1996_08
ORD IDord-657984d3743a4ef6977540748962a198
Source noteuspto-grants-1996_08