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HRID 278480作成日:2026年10月26日

Imidazole → Methyl 3-[4-(tert-butyldimethylsilyloxy)-3-oxobutyl]phenylacetate

https://huagongshe.com/reaction/278480

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物tert-Butyldimethylsilyl chlorideHCID 28928—
反応物Methyl 3-(4-hydroxy-3-oxobutyl)phenylacetateHCID 22628477—
溶媒DimethylformamideHCID 6228—
生成物Methyl 3-[4-(tert-butyldimethylsilyloxy)-3-oxobutyl]phenylacetateHCID 2262845994.9%

反応手順

To an ice cooled solution of methyl 3-(4-hydroxy-3-oxo-butyl)phenylacetate (472 mg, 2.00 mmol) in DMF (10 ml) was added imidazole (264 mg, 3.88 mmol) followed by tert-butyldimethylsilyl chloride (408 mg, 5.99 mmol). After 30 minutes the ice-bath was removed and then the mixture was stirred overnight at room temperature. The reaction mixture was poured into water (100 ml) and extracted with ethyl acetate. The organic layer was washed with brine, dried (magnesium sulfate), and concentrated in vacuo. The residue was purified by silica gel (20 g) column chromatography eluting with hexane/ethyl acetate (10:1) to give methyl 3-[4-(tert-butyldimethylsilyloxy)-3-oxobutyl]phenylacetate (664 mg, 94.9%) as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06359145B1
出典データセットuspto-grants-2002_03
ORD IDord-b774a9a2e1924066b5eae6f3b0d8fa73
出典メモuspto-grants-2002_03