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HRID 581609作成日:2026年10月25日

TMS-Imidazole → (4aS,8aR)-5-[(R)-5-Trimethylsilanyloxy-1,5-dimethyl-hex-3-ynyl]-4a-methyl-1,2,3,4,4a,7,8,8a-octahydro-naphthalen-1-one

https://huagongshe.com/reaction/581609

反応式

関与物質

役割名称HCID仕込み量
反応物TMS-ImidazoleHCID 14420972—
反応物(4aS,8aR)-5-((R)-5-Hydroxy-1,5-dimethyl-hex-3-ynyl)-4a-methyl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-oneHCID 57031123—
溶媒DichloromethaneHCID 6344—
生成物(4aS,8aR)-5-[(R)-5-Trimethylsilanyloxy-1,5-dimethyl-hex-3-ynyl]-4a-methyl-1,2,3,4,4a,7,8,8a-octahydro-naphthalen-1-oneHCID 67613097—

反応手順

446 mg (1.55 mmol) of (4aS,8aR)-5-((R)-5-hydroxy-1,5-dimethyl-hex-3-ynyl)-4a-methyl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-one in 12 ml of abs. CH2Cl2 was treated with 2.03 ml (9 eq.) of TMS-imidazole and kept at RT for 24 h. Pouring onto crushed ice, twofold extraction with ether, washing with water and brine, and drying over sodium sulfate left a crude product, which was purified by flash chromatography (SiO2, hexane/AcOEt=9/1). Thereby, 561 mg of the title compound was obtained as colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05919986
出典データセットuspto-grants-1999_07
ORD IDord-2a4b6d95962147b2ac4a05cf0cfd6b68
出典メモuspto-grants-1999_07