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HRID 413609作成日:2026年10月24日

p-Toluenesulfonic acid → (1s,3r,6r,10r)-3-(4'-Methoxyphenyl)-10-hydroxy-2,4,7-trioxabicyclo[4.4.0]decane

https://huagongshe.com/ja/reaction/413609

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物TriethylamineHCID 8471—
反応物Ethyl AcetateHCID 8857—
反応物DimethylacetamideHCID 31374—
反応物p-(Dimethoxymethyl)anisoleHCID 75140—
生成物(1s,3r,6r,10r)-3-(4'-Methoxyphenyl)-10-hydroxy-2,4,7-trioxabicyclo[4.4.0]decaneHCID 20588607—

反応条件

温度62.5 °C

反応手順

5.0 g (33.8 mmol) of 2 and 8.30 g (45.8 mmol) of p-methoxybenzaldehyde dimethyl acetal were dissolved in 50 ml of anhydrous DMA, and a catalytic amount of 4-toluenesulfonic acid was added until the mixture was acidic. The reaction solution was agitated for about 5 hours in a rotary evaporator at 60-65° C. and a reduced pressure of 30 mbar. The reaction solution was neutralized using triethylamine. 300 ml of ethyl acetate were added, and the mixture was extracted three times with water. The organic phase was dried over Na2SO4, the drying agent was filtered off, and the residue was evaporated under reduced pressure. The crude product was dissolved in a little ethyl acetate, precipitated using n-hexane, filtered off with suction and dried under reduced pressure.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06569355B1
出典データセットuspto-grants-2003_05
ORD IDord-63a9c62168864f38bdd617b0cdcec539
出典メモuspto-grants-2003_05