Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6457생성일: 2026년 10월 24일
Water → (4R-cis) 1,1-dimethylethyl 6-(2-nitrobenzenesulfonyloxymethyl)-2,2-dimethyl-1,3-dioxane-4-acetate
https://huagongshe.com/ko/reaction/6457
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 2-Nitrobenzenesulfonyl chloride | HCID 15540 | — |
| 반응물 | tert-Butyl 2,4-dideoxy-3,5-O-(1-methylethylidene)-D-erythro-hexonate | HCID 9816650 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (4R-cis) 1,1-dimethylethyl 6-(2-nitrobenzenesulfonyloxymethyl)-2,2-dimethyl-1,3-dioxane-4-acetate | HCID 54107594 | 122.9% |
반응 단계
To a stirring 20°-25° C. solution of the (4R cis)-1,1-dimethylethyl 6-hydroxymethyl-2,2-dimethyl -1,3-dioxane-4-acetate (European Patent Application 0319,847) (10 g, 0.038 mol) in methylene chloride (250 mL) containing triethylamine (7 mL, 0.05 mol) is added 2-nitrobenzenesulfonyl chloride (9.8 g, 0.043 mol). Stirring is continued at 20°-25° C. for 24 hours, a further portion of 2-nitrobenzenesulfonyl chloride (2.0 g, 0.009 mol) is added and the solution stirred for a further 4 hours. The solution is then poured onto 200 mL of water and the layers separated. The upper aqueous layer is extracted with 250 mL of methylene chloride and the combined organic layers are washed with 100 mL each of saturated sodium bicarbonate solution to ensure complete removal of 2-nitrobenzenesulfonyl chloride and then saturated sodium chloride. Drying the solution with magnesium sulfate and concentration in vacuo gives 20.8 g of the product as a green oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05248793 |
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| 출처 데이터셋 | uspto-grants-1993_09 |
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| ORD ID | ord-f0db01e0d32e4cd2b57589e37275a000 |
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| 출처 메모 | uspto-grants-1993_09 |
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