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HRID 656208作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/656208

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—

反応条件

温度0 °C

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° C. The reaction mixture was warmed to 0° C. 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US08071635B2
出典データセットuspto-grants-2011_12
ORD IDord-cbb4a56e9ade4183acb257439426d48b
出典メモuspto-grants-2011_12