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HRID 655077作成日:2026年10月26日

Imidazole → (E)-3-[2(tert-Butyl-dimethyl-silanoxy)-phenyl]-acrylic acid

https://huagongshe.com/reaction/655077

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物Lithium HydroxideHCID 3939—
反応物tert-Butyldimethylsilyl chlorideHCID 28928—
反応物O-Coumaric AcidHCID 637540—
溶媒DimethylformamideHCID 6228—
溶媒Oxolane--water (1/1)HCID 21881883—
生成物(E)-3-[2(tert-Butyl-dimethyl-silanoxy)-phenyl]-acrylic acidHCID 2229046253.9%

反応手順

To a solution of 8.2 g of (E)-3-(2-hydroxy-phenyl)-acrylic acid and 15.2 g of TBDMS-Cl in 10 ml of DMF was added 11.9 g of imidazole and the mixture was stirred at room temperature for 24 h. After aqueous work-up, the bis-silylated product was saponified with 2.1 g of LiOH in THF-H2O for 0.5 h at 0° C. The mixture was concentrated in vacuo and TBDMS-OH removed by extraction with hexane. The aqueous layer was acidified to pH 4 with KHSO4 and extracted with EtOAc. The organic phases were washed with brine, dried (Na2SO4) and evaporated to dryness. The semi-solid residue was suspended in hexane, filtered and the filtrate evaporated to dryness to yield 7.5 g of a pale yellow oil, which solidified upon standing.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号USRE043006E1
出典データセットuspto-grants-2011_12
ORD IDord-66880a3a91f5458492c6643a8c152417
出典メモuspto-grants-2011_12