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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795694Generated: October 29, 2026

Ethyl Acetate → HCID 86604546, compound

https://huagongshe.com/reaction/1795694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant3-Pyridinecarbonyl chloride, hydrochloride (1:1)HCID 88438—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant(8E,12E,14E)-3,6,21-Tri(1-ethoxyethoxy)-7-hydroxy-6,10,12,16,20-pentamethyl-18,19-epoxytricosa-8,12,14-trien-11-olideHCID 21023947—
CatalystHCID 68666183HCID 68666183—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86604546HCID 8660454667%

Reaction Steps

Lithium bis(trimethylsilyl)amide (1.0 M tetrahydrofuran solution, 50 μL, 50 μmol) was added dropwise to a solution of (8E,12E,14E)-3,6,21-tri(1-ethoxyethoxy)-7-hydroxy-6,10,12,16,20-pentamethyl-18,19-epoxytricosa-8,12,14-trien-11-olide (10.8 mg, 15.2 μmol) in tetrahydrofuran (2 mL) at −40° C. under nitrogen atmosphere, followed by stirring at the same temperature for 20 min. Then, a solution of nicotinoyl chloride hydrochloride (5.7 mg, 30.4 μmol) in tetrahydrofuran-triethylamine (tetrahydrofuran: 0.5 mL and triethyamine: 1 drop) was added dropwise thereinto, followed by stirring at 0° C. for 30 min. Ethyl Acetate and water were added to the reaction solution, and the mixture was extracted with ethyl acetate. The resulting organic layer was dried over anhydrous magnesium sulfate, filtered and then evaporated. The resulting residue was purified by silica gel column chromatography (Kanto silica gel 60N, 40 to 50 μm; ethyl acetate-hexane=1:4) to obtain the title compound (6.3 mg, 67%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07026352B1
Source datasetuspto-grants-2006_04
ORD IDord-98b27fa8049545cb9e21ef2a880782d4
Source noteuspto-grants-2006_04