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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1456551Generated: November 4, 2026

Ethyl Acetate → HCID 67584325, compound

https://huagongshe.com/reaction/1456551

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant4-Fluoro-2-[2-(4-fluorophenyl)ethyl]phenolHCID 22106952—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 57301849HCID 57301849—
SolventDimethylacetamideHCID 31374—
ProductHCID 67584325HCID 6758432574%

Reaction Steps

687 mg of 4-fluoro-2-[2-(4-fluorophenyl)ethyl]phenol (prepared as described in Preparation 6) were dissolved in 12 ml of N,N-dimethylacetamide, and then 212 mg of potassium t-butoxide were added to the resulting solution, whilst ice-cooling. The resulting mixture was then stirred for 10 minutes, after which 687 mg of (2S,4R)-2-(2-chloroethyl)-1-t-butoxycarbonyl-4-t-butyldimethylsilyloxypyrrolidine were added. The resulting mixture was then stirred at room temperature for 14 hours. At the end of this time, 135 mg of potassium t-butoxide were added to the reaction mixture, and the mixture was stirred at 40° C. for 4 hours, after which 300 ml of ethyl acetate were added. The resulting reaction mixture was washed with water and with a saturated aqueous solution of sodium chloride, in that order. The ethyl acetate layer was separated and dried over anhydrous magnesium sulfate. It was then concentrated by evaporation under reduced pressure. The resulting oily substance was purified by silica gel column chromatography, using a 2:3 by volume mixture of hexane and ethyl acetate as the eluent, to give 571 mg (yield 74%) of the title compound as a colorless oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05843983
Source datasetuspto-grants-1998_12
ORD IDord-9b3e34053f2142b590ce0b374d842f97
Source noteuspto-grants-1998_12