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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2265097Generated: October 25, 2026

Ethyl 4-[[3,5-bis(trimethylsilyl)benzoyl]amino]-2-fluorocinnamate → (E)-Ethyl 3-[4-[[3,5-bis(trimethylsilyl)benzoyl]amino]-2,5-difluorophenyl]-2-butenoate

https://huagongshe.com/reaction/2265097

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-[[3,5-bis(trimethylsilyl)benzoyl]amino]-2-fluorocinnamateHCID 68484203—
Reactant(E)-Ethyl 3-(4-amino-2,5-difluorophenyl)-2-butenoateHCID 86644278—
Product(E)-Ethyl 3-[4-[[3,5-bis(trimethylsilyl)benzoyl]amino]-2,5-difluorophenyl]-2-butenoateHCID 8664427946%

Reaction Steps

BTMB (800 mg) and Compound 10a (869 mg) were reacted in the same manner as Compound 2b was synthesized. After the reaction was over, the reaction mixture was separated with ethyl acetate and water. The organic layer was washed once with water and once with a saturated sodium chloride solution, and then dried over anhydrous sodium sulfate. The solvent was distilled off, and the residue was purified by column chromatography (5% ethyl acetate/n-hexane) to obtain Compound 10b (674 mg, 46%) as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855300B2
Source datasetuspto-grants-2010_12
ORD IDord-8891bfeb29be478581e150da1efe3786
Source noteuspto-grants-2010_12