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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1838370생성일: 2026년 10월 27일

Water → (1-(4-Fluorobenzyl)-5-methanesulfonylindol-2-yl)-methanol

https://huagongshe.com/reaction/1838370

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Aluminium lithium hydrideHCID 21226445—
반응물1-(4-fluorobenzyl)-5-methanesulfonylindole-2-carboxylic Acid Methyl EsterHCID 68444704—
용매TetrahydrofuranHCID 8028—
생성물(1-(4-Fluorobenzyl)-5-methanesulfonylindol-2-yl)-methanolHCID 22504394104.9%

반응 단계

To a solution of lithium aluminum hydride (366 mg) in tetrahydrofuran (20 ml), a solution of 1-(4-fluorobenzyl)-5-methanesulfonylindole-2-carboxylic acid methyl ester obtained in Example 27 (3) (1.86 g) in tetrahydrofuran (20 ml) was added dropwise at 0° C. under nitrogen atmosphere and the mixture was stirred at the same temperature for 30 minutes. The reaction solution was poured into water, filtered through Celite and extracted with chloroform. The organic layer was washed with water and dried. The solvent was distilled off under reduced pressure to obtain (1-(4-fluorobenzyl)-5-methanesulfonylindol-2-yl)-methanol (1.8 g). To a solution of the resulting alcohol (1.8 g) in dichloromethane (100 ml) was added manganese dioxide (15.3 g) at 15 to 30° C. and the mixture was stirred at the same temperature for 30 minutes. The reaction solution was filtered through Celite. The solvent was distilled off under reduced pressure to obtain 1.5 g (88.4%) of the desired product as a yellow powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06673797B1
출처 데이터셋uspto-grants-2004_01
ORD IDord-a5c7bf32bc3b4d2f9dd0f9ed0c7a4b35
출처 메모uspto-grants-2004_01