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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 388744생성일: 2026년 10월 25일

Acetic Acid → (1s,3s,5r,6s)-5-{[Tert-butyl(dimethyl)silyl]oxy}-6-methyl-7-oxabicyclo[4.1.0]heptan-3-ol

https://huagongshe.com/reaction/388744

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Potassium CarbonateHCID 11430—
반응물(1s,3s,5r,6s)-5-{[Tert-butyl(dimethyl)silyl]oxy}-6-methyl-7-oxabicyclo[4.1.0]hept-3-yl acetateHCID 87629193—
용매MethanolHCID 887—
생성물(1s,3s,5r,6s)-5-{[Tert-butyl(dimethyl)silyl]oxy}-6-methyl-7-oxabicyclo[4.1.0]heptan-3-olHCID 8762883098%

반응 단계

The compound of Example 16C (9.20 g, 30.6 mmol) was dissolved in 105 mL of methanol. K2CO3 (10.1 g, 72.1 mmol, 2.35 equivalents) was added and the reaction mixture was stirred at ambient temperature for 2 hours. 6.60 mL (115 mmol, 3.77 equivalents) of acetic acid were added to the reaction mixture; after mixing for 10 minutes, the solids were filtered off and rinsed with 40 mL of methanol. The combined filtrate and rinses were concentrated to a residue which was mixed with 106 mL of water. The layers were separated, and the aqueous layer was extracted three times with 50 mL of ethyl acetate. The combined organic layers were washed twice with 45 mL of brine, dried over MgSO4, filtered and concentrated to afford the titled compound (7.72 g, 98%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08377913B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-2613d346a3a24dd887853b5dc7d0b75a
출처 메모uspto-grants-2013_02