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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 560166생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/560166

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Triisopropylsilyl trifluoromethanesulfonateHCID 2724529—
반응물4-(2-Hydroxyethyl)cyclohexan-1-oneHCID 15700392—
용매DichloromethaneHCID 6344—
생성물4-(2-Triisopropylsilanyloxy-ethyl)-cyclohexanoneHCID 21986099—

반응 단계

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)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08063086B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-f60e6841a2bd4bf0b9cfbb1d1c7810c3
출처 메모uspto-grants-2011_11