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HRID 2252950作成日:2026年10月25日

Diisopropylethylamine → 4-(2-Triisopropylsilanyloxy-ethyl)-cyclohexanone

https://huagongshe.com/reaction/2252950

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物Triisopropylsilyl trifluoromethanesulfonateHCID 2724529—
反応物4-(2-Hydroxyethyl)cyclohexan-1-oneHCID 15700392—
溶媒DichloromethaneHCID 6344—
生成物4-(2-Triisopropylsilanyloxy-ethyl)-cyclohexanoneHCID 21986099—

反応手順

A solution of 4-(2-hydroxy-ethyl)-cyclohexanone (Intermediate R10, 6.8 g, 52.6 mmol, (obtainable as described in the publication by Ciufolini et. al. J. Amer. Chem. Soc. 1991, 113, 8016) was dissolved in CH2Cl2 (75 mL) and treated with diisopropylethylamine (9.2 mL, 52.6 mmol) followed by tri-isopropylsilyl trifluoromethane sulfonate (TIPSTf) (15.3 g, 50.2 mmol) at −30 EC. The reaction mixture was warmed to 0 EC for 1 h. The mixture was subjected to an aqueous work-up and purified by chromatography on SiO2 to give 4-(2-triisopropylsilanyloxy-ethyl)-cyclohexanone (Intermediate R11, 11.8 g (82%). Intermediate R11 was converted via Intermediate R12 to the unsaturated aldehyde, 5-(2-triisopropylsilanyloxy-ethyl)-cyclohex-1-enecarbaldehyde (Intermediate R13)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07323485B2
出典データセットuspto-grants-2008_01
ORD IDord-59b2d039da4c48ea8c2b1a6a13a22693
出典メモuspto-grants-2008_01