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HRID 348248作成日:2026年10月24日

Iodine → (5R)-2-iodo-6-methyl-7-(2-methylthiazol-4-yl)-5-(triethylsilyloxy)-2,6-heptadiene

https://huagongshe.com/ja/reaction/348248

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物Sodium bis(trimethylsilyl)amideHCID 2724254—
反応物(3R)-3-(triethylsilyloxy)-4-methyl-5-(2-methylthiazol-4-yl)-pent-4-enalHCID 86586609—
反応物ButyllithiumHCID 178418339—
触媒Ethyltriphenylphosphonium iodideHCID 78474—
溶媒PentaneHCID 8003—
溶媒TetrahydrofuranHCID 8028—
生成物(5R)-2-iodo-6-methyl-7-(2-methylthiazol-4-yl)-5-(triethylsilyloxy)-2,6-heptadieneHCID 86586611—

反応条件

温度-30 °C

反応手順

To a suspension of ethyltriphenylphosphonium iodide (7.90 g) in THF (150 mL) is added n-butyllithium (7.17 mL, 2.5 M in hexane) at ambient temperature. After disappearance of the solid material, the red solution is cannulated into a vigorously stirred solution of iodine (4.54 g) in THF (150 mL) at −78° C. The resulting dark brown suspension is stirred for 5 minutes and allowed to warm gradually to −30° C. A solution of sodium hexamethyldisilazide (17.3 mL, 1.0 M in THF) is added dropwise to afford a dark red solution. A solution of (3R)-3-(triethylsilyloxy)-4-methyl-5-(2-methylthiazol-4-yl)-pent-4-enal (2.0 g) in THF (10 mL) is slowly added, and stirring is continued at −30° C. for 30 minutes. The reaction mixture is diluted with pentane (100 mL), filtered through a pad of Celite, and concentrated. Purification by flash column chromatography on SiO2 (hexane/ethyl acetate, 15:1) affords the vinyl iodide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07176235B2
出典データセットuspto-grants-2007_02
ORD IDord-a5069b305f724da99decc21ed307992b
出典メモuspto-grants-2007_02