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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1295551생성일: 2026년 10월 26일

1-o-Methyl-2-methyl-3,5-bis-o-(2,4-dichlorobenzyl)-beta-d-ribofuranose → 1-o-Methyl-3,5-bis-o-(2,4-dichlorobenzyl)-beta-d-ribofuranose

https://huagongshe.com/reaction/1295551

반응식

참여 물질

역할이름HCID투입량
반응물1-o-Methyl-2-methyl-3,5-bis-o-(2,4-dichlorobenzyl)-beta-d-ribofuranoseHCID 21040816—
용매DichloromethaneHCID 6344—
생성물1-o-Methyl-3,5-bis-o-(2,4-dichlorobenzyl)-beta-d-ribofuranoseHCID 67435068—

반응 조건

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 번호US07244713B2
출처 데이터셋uspto-grants-2007_07
ORD IDord-49e01139168c44119d68b0be19688782
출처 메모uspto-grants-2007_07