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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1270049생성일: 2026년 10월 25일

beta-D-Ribofuranoside, methyl 2,3,5-tris-O-[(2,4-dichlorophenyl)methyl]- → 1-o-Methyl-3,5-bis-o-(2,4-dichlorobenzyl)-beta-d-ribofuranose

https://huagongshe.com/reaction/1270049

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참여 물질

역할이름HCID투입량
반응물beta-D-Ribofuranoside, methyl 2,3,5-tris-O-[(2,4-dichlorophenyl)methyl]-HCID 11767425—
용매DichloromethaneHCID 6344—
생성물1-o-Methyl-3,5-bis-o-(2,4-dichlorobenzyl)-beta-d-ribofuranoseHCID 67435068—

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온도3 °C

반응 단계

To a solution of the product of Step 1 (171.60 g, 0.2676 mol) in 1.8 L of methylene chloride that was cooled to 0° C., was added dropwise a solution of stannous chloride (31.522 mL, 0.2676 mol) in 134 mL of methylene chloride while stirring. After maintaining the solution at about 3° C. for approximately 27 hours, another 5.031 mL of stannous chloride (SnCl4) (0.04282 mol) was added and the solution was kept at about 3° C. overnight. After a total reaction time of approximately 43 hours, the reaction was quenched by carefully adding the solution to 1.9 L of a saturated NaHCO3 solution. Tin salts were removed via filtration through Celite after which the organic phase was isolated, dried with MgSO4 and evaporated in vacuo. The yield of raw, dark yellow oil was 173.6 g. The crude oil was used directly in the next step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07202223B2
출처 데이터셋uspto-grants-2007_04
ORD IDord-0218ea5a44084fdabfd7e4f77d0ae961
출처 메모uspto-grants-2007_04