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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2115598생성일: 2026년 10월 26일

Imidazole → 4-(Tert-butyl-dimethyl-silanyloxymethyl)-1-cycloheptyl-pyrrolidine-2-one

https://huagongshe.com/reaction/2115598

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물Phosphoric AcidHCID 1004—
반응물Ethyl AcetateHCID 8857—
반응물tert-Butyldimethylsilyl chlorideHCID 28928—
반응물Sodium borohydrideHCID 4311764—
반응물1-Cycloheptyl-5-oxo-pyrrolidine-3-carboxylic acid methyl esterHCID 66656958—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물4-(Tert-butyl-dimethyl-silanyloxymethyl)-1-cycloheptyl-pyrrolidine-2-oneHCID 131727092—

반응 조건

온도60 °C

반응 단계

Sodium borohydride (0.213 g, 5.77 mmoles) was added to a solution of Example 1A (0.7 g, 2.92 mmoles) in methanol (3 mL) and tetrahydrofuran (3 mL) and stirred at 60° C. for two hours. The reaction was cooled to 0° C. and O-phosphoric acid (1.6 g, 17.4 mmoles) was added and stirred. The reaction was filtered through a pad of celite, rinsed with methanol, and concentrated under vacuo. The crude oil was taken up in ethyl acetate (25 mL) and washed with water (25 mL). The organic layer was dried with MgSO4, filtered and evaporated in vacuo. The resulting oil was taken up in N,N-dimethylformamide (4 mL) and imidazole (391 g, 5.76 mmoles) and Tert-butyl-chloro-dimethyl-silane (583 g, 3.88 mmoles) were added and stirred for three hours. The reaction was diluted with ethyl acetate (40 mL) and washed with water (50 mL) and brine (25 mL). The organic layer was dried with MgSO4 filtered and evaporated in vacuo. The crude product was purified by flash chromatography (hexanes:ethyl acetate 95:5 to 75:25) to give the title compound as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07435833B2
출처 데이터셋uspto-grants-2008_10
ORD IDord-1a128a5192af43cda51ebde3c80bd194
출처 메모uspto-grants-2008_10