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HRID 1270049作成日:2026年10月24日

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/ja/reaction/1270049

反応式

関与物質

役割名称HCID仕込み量
反応物beta-D-Ribofuranoside, methyl 2,3,5-tris-O-[(2,4-dichlorophenyl)methyl]-HCID 11767425—
溶媒DichloromethaneHCID 6344—
生成物1-o-Methyl-3,5-bis-o-(2,4-dichlorobenzyl)-beta-d-ribofuranoseHCID 67435068—

反応条件

温度3 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07202223B2
出典データセットuspto-grants-2007_04
ORD IDord-0218ea5a44084fdabfd7e4f77d0ae961
出典メモuspto-grants-2007_04