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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475428Generated: October 29, 2026

Ethyl orthoformate → HCID 66847930, compound

https://huagongshe.com/reaction/475428

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl orthoformateHCID 31214—
Reactant2-(6-Bromobenzo[d]isoxazol-3-yl)benzaldehydeHCID 86675995—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventEthanolHCID 702—
ProductHCID 66847930HCID 66847930101.2%

Reaction Conditions

Temperature45 °C

Reaction Steps

To a stirred suspension of 2-(6-bromobenzo[d]isoxazol-3-yl)benzaldehyde (Compound 4a) (10 g) in dry ethanol (100 mL) was added p-toluenesulfonic acid (0.315 g) followed by triethyl orthoformate (11.01 mL, 9.81 g). The suspension was stirred at 45° C. until a clear solution resulted and then maintained at 45° C. for 45 min. The solvent was removed under vacuum and then the mixture was diluted with ethyl acetate and then washed with saturated sodium carbonate solution, brine and then dried over anhydrous sodium sulfate, filtered and evaporated to give the title product (12.6 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637551B2
Source datasetuspto-grants-2014_01
ORD IDord-75172dc3bc1f4a749e9bfecad9efacab
Source noteuspto-grants-2014_01