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HRID 38304作成日:2026年10月25日

Dimethyl Sulfate → 4-methoxy-3-[3-[3-chloro-4-(trifluoromethoxy)phenyl]-1-oxo-2-propenyl]-2H-1-benzopyran-2-one

https://huagongshe.com/reaction/38304

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfateHCID 6497—
反応物Sodium hydrideHCID 24758—
反応物4-hydroxy-3-[3-[3-chloro-4-(trifluoromethoxy)phenyl]1-oxo-2-propenyl]-2H-1-benzopyran-2-oneHCID 76211114—
溶媒HexamethylphosphoramideHCID 12679—
生成物4-methoxy-3-[3-[3-chloro-4-(trifluoromethoxy)phenyl]-1-oxo-2-propenyl]-2H-1-benzopyran-2-oneHCID 74019991—

反応手順

In 15 ml of hexamethylphosphoramide was dissolved 1.37 g of 4-hydroxy-3-[3-[3-chloro-4-(trifluoromethoxy)phenyl]1-oxo-2-propenyl]-2H-1-benzopyran-2-one, to this solution was added 0.17 g of sodium hydride (60% oily), and this was stirred at room temperature for 30 minutes. Then, 0.8 ml of dimethyl sulfate, and this was stirred at 65° C. for 2 hours. Thereafter, the reaction mixture was added to ice water, and this was extracted with ethyl acetate. The organic layer was washed with an aqueous saturated sodium chloride solution, dried with anhydrous magnesium sulfate, and concentrated. The residue was washed with t-butyl methyl ether to obtain 0.38 g of 4-methoxy-3-[3-[3-chloro-4-(trifluoromethoxy)phenyl]-1-oxo-2-propenyl]-2H-1-benzopyran-2-one [Compound No. (2c-17)] as a pale yellow crystal.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524729B2
出典データセットuspto-grants-2013_09
ORD IDord-75dfcb2215cb4145b0e850ce7d13f174
出典メモuspto-grants-2013_09