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HRID 403011作成日:2026年10月27日

Iodine → 3,4-Dibenzyloxy-6-iodobenzyl alcohol

https://huagongshe.com/reaction/403011

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物3,4-Bis(benzyloxy)benzyl alcoholHCID 74338—
触媒Silver trifluoroacetateHCID 76299—
溶媒ChloroformHCID 6212—
生成物3,4-Dibenzyloxy-6-iodobenzyl alcoholHCID 6673355084%

反応手順

The dibenzyloxybenzyl alcohol 28 (21.44 mmol) and silver trifluoroacetate (21.44 mmol) were suspended in 100 mL of dry chloroform and stirred under argon. A solution of iodine (21.44 mmol) in dry chloroform (50 mL) was added to the suspension dropwise at room temperature. The reaction mixture was then stirred for a further period of 2 h and filtered. The filtrate was washed with 20% sodium thiosulfate solution in water. The organic layer was separated and dried over anhydrous Na2SO4. Filtration was followed by evaporation of the chloroform solution resulting in the pure iodo compound, 3,4-Dibenzyloxy-6-iodobenzyl alcohol (29), as a pale yellow solid in 84% yield.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08742139B2
出典データセットuspto-grants-2014_06
ORD IDord-ecb27ec953764accb3730e698a8568d6
出典メモuspto-grants-2014_06