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HRID 22521作成日:2026年10月25日

Dimethyl Sulfide → HCID 131717895、化合物

https://huagongshe.com/reaction/22521

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfideHCID 1068—
反応物Dichloromethane methanolHCID 21226129—
反応物N-[2-(1,3-Dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-oxo-3-phenylpropyl]-O-2-propenyl-L-serine, methyl esterHCID 70044917—
生成物HCID 131717895HCID 131717895—

反応条件

温度-78 °C

反応手順

Dissolve N-[2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-oxo-3-phenylpropyl]-O-2-propenyl-L-serine, methyl ester (13 g, 29.8 mmol ) in methylene chloride/methanol (10:1, 220 mL). Cool to -78° C. and sparge with a mixture of ozone/oxygen for approximately 10 minutes until a blue color persists. Sparge with nitrogen for 10 minutes at -78° C. to remove excess ozone. Treat with methylsulfide (60 mL, 0.82 mol) and allow to warm to room temperature. Stir at room temperature for 2.5 hours, evaporate the solvent in vacuo and dissolve the residue in ethyl acetate (200 mL). Wash with water, saturated sodium chloride, dry (Mg SO4) and evaporate the solvent in vacuo to give the intermediate N-[2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-oxo-3-phenylpropyl]-O-2-oxoethyl-L-serine, methyl ester as a foam (13.6 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05428158
出典データセットuspto-grants-1995_06
ORD IDord-5c8da73e210d40aaa7b93f90ddc1afb7
出典メモuspto-grants-1995_06