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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814108Generated: October 25, 2026

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

https://huagongshe.com/reaction/1814108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAluminium lithium hydrideHCID 21226445—
Reactant1-(4-fluorobenzyl)-5-methanesulfonylindole-2-carboxylic Acid Methyl EsterHCID 68444704—
SolventTetrahydrofuranHCID 8028—
Product(1-(4-Fluorobenzyl)-5-methanesulfonylindol-2-yl)-methanolHCID 22504394104.9%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875770B2
Source datasetuspto-grants-2005_04
ORD IDord-d18c1d47eb1f4c508d962120715c500c
Source noteuspto-grants-2005_04