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HRID 465138作成日:2026年10月26日

Imidazole → 3alpha-(t-Butyldimethylsilyloxy)-7alpha,12alpha-dihydroxy-5beta-cholan-24-oic acid

https://huagongshe.com/reaction/465138

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物WaterHCID 962—
反応物tert-Butyldimethylsilyl chlorideHCID 28928—
反応物Cholic AcidHCID 221493—
溶媒DimethylformamideHCID 6228—
生成物3alpha-(t-Butyldimethylsilyloxy)-7alpha,12alpha-dihydroxy-5beta-cholan-24-oic acidHCID 70479218—

反応手順

Cholic acid, 4.08 g, is dissolved in 10 ml of dry dimethylformamide and 3.40 g of imidazole is added, followed by 3.60 g of t-butyldimethylsilyl chloride. The reaction mixture is allowed to stand overnight at room temperature. The reaction mixture is poured into water, filtered and the precipitate is washed with water. This precipitate is dissolved in 30 ml of tetrahydrofuran and 3 ml of water and 2 ml of acetic acid is added. After 6.5 hours, the solvent is evaporated and the residue chromatographed on 200 g of silica gel with 5% methanol in methylene chloride as eluent, to provide 3α-(t-butyldimethylsilyloxy)-7α,12α-dihydroxy-5β-cholan-24-oic acid, mp 145.5°-148, having the following structural formula: ##STR15##

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04550163
出典データセットuspto-grants-1985_10
ORD IDord-f6006852e2ce436f95dca7212a259a8a
出典メモuspto-grants-1985_10