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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704612Generated: October 31, 2026

Ethyl Acetate → HCID 67804591, compound

https://huagongshe.com/reaction/704612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantAmmonium ChlorideHCID 25517—
ReactantBromotrimethylsilaneHCID 76113—
ReactantHCID 131716766HCID 131716766—
SolventDichloromethaneHCID 6344—
SolventDCM MeOH AcOHHCID 21877243—
ProductHCID 67804591HCID 6780459135%

Reaction Steps

Under an atmosphere of argon, 29 μl (0.22 millimole) of bromotrimethylsilane was added to a solution of 48 mg (0.11 millimole) of phthalidyl (Z)-3-cyclohexyl-2-(ethoxyisobutylphosphinoyl)methylpropenoate in 0.50 ml of dry dichloromethane, and the mixture was stirred at room temperature for 18 hours. To the reaction mixture were added 2.0 ml of ethyl acetate and 3.0 ml of a saturated aqueous solution of ammonium chloride, and the mixture was stirred at room temperature for 30 minutes. A saturated aqueous solution of ammonium chloride (3 ml) was added to the reaction mixture, and the mixture was extracted three times with 8 ml of ethyl acetate each time. The combined organic layers were dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by preparative thin-layer chromatography [silica gel 60 F254 made by E. Merck & Co.; dichloromethane/methanol/acetic acid (30:1:1)]to give 16 mg (yield 35%) of the captioned compound as a colorless oil. On standing, this compound solidified.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04988681
Source datasetuspto-grants-1991_01
ORD IDord-008f739e991b4721b343c6d2581cd1d3
Source noteuspto-grants-1991_01