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HRID 567413作成日:2026年10月25日

Dichloromethane → (7R)-2-acetoxymethyl-7-[(1R,7aR)-octahydro-4-trimethylsilyloxy-7a-methyl-1H-inden-1-yl]-octen-4-ol

https://huagongshe.com/reaction/567413

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物2-(Trimethylsilylmethyl)allyl acetateHCID 4428347—
反応物(4R)-4-[(1R,7aR)-octahydro-4-trimethylsilyloxy-7a-methyl-1H-inden-1-yl]-pentanalHCID 57264692—
溶媒TriethylamineHCID 8471—
生成物(7R)-2-acetoxymethyl-7-[(1R,7aR)-octahydro-4-trimethylsilyloxy-7a-methyl-1H-inden-1-yl]-octen-4-olHCID 5708627957%

反応条件

温度-78 °C

反応手順

A 1.72 g amount of the compound (4-7), (4R)-4-[(1R,7aR)-octahydro-4-trimethylsilyloxy-7a-methyl-1H-inden-1-yl]-pentanal and 1.10 g of 2-(trimethylsilyl-methyl)-2-propenyl acetate were taken in a 200 ml eggplant-shaped flask, then 30 ml of dichloromethane was added and the solution stirred at −78° C. To this was added 0.86 ml of BF•Et2O, then the solution stirred at −78° C. for 1 hour. Further, 3 ml of triethylamine was added to stop the reaction, then the solvent was distilled off under reduced pressure. The obtained residue was purified by a silica gel column (IR-60, 150 g, hexane/ethyl acetate=50/1 to 9/1) to obtain the desired product (4-8), (7R)-2-acetoxymethyl-7-[(1R,7aR)-octahydro-4-trimethylsilyloxy-7a-methyl-1H-inden-1-yl]-octen-4-ol in an amount of 1.32 g (yield 57%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06177586B1
出典データセットuspto-grants-2001_01
ORD IDord-fa65f8ce7af54430bbb307309ab36613
出典メモuspto-grants-2001_01