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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 1-(4-fluorobenzyl)-5-methanesulfonylindole-2-carboxylic Acid Methyl Ester | HCID 68444704 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (1-(4-Fluorobenzyl)-5-methanesulfonylindol-2-yl)-methanol | HCID 22504394 | 104.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06875770B2 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-d18c1d47eb1f4c508d962120715c500c |
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| Source note | uspto-grants-2005_04 |
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