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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | (1s,3s,5r,6s)-5-{[Tert-butyl(dimethyl)silyl]oxy}-6-methyl-7-oxabicyclo[4.1.0]hept-3-yl acetate | HCID 87629193 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | (1s,3s,5r,6s)-5-{[Tert-butyl(dimethyl)silyl]oxy}-6-methyl-7-oxabicyclo[4.1.0]heptan-3-ol | HCID 87628830 | 98% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08377913B2 |
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| 출처 데이터셋 | uspto-grants-2013_02 |
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| ORD ID | ord-2613d346a3a24dd887853b5dc7d0b75a |
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| 출처 메모 | uspto-grants-2013_02 |
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