HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434113Generated: October 28, 2026
HCID 9899948, compound → 5-chloro-2-fluoro-2-methanesulfonyl-1-methylindan-1-ol
https://huagongshe.com/reaction/434113
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 9899948 | HCID 9899948 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-chloro-2-fluoro-2-methanesulfonyl-1-methylindan-1-ol | HCID 9835372 | — |
Reaction Steps
At room temperature, 260 mg (1 mmol) of 5-chloro-2-fluoro-2-methanesulfonylindan-1-one are dissolved in 10 ml of dry tetrahydrofuran, and 0.33 ml of a 3M solution of methylmagnesium bromide in diethyl ether is added dropwise with stirring. The reaction mixture is stirred at 50° C. for 3 h. A further 0.33 ml of the methylmagnesium bromide solution is then added, and the mixture is stirred at room temperature for another hour. After the reaction has ended, the reaction mixture is diluted with ethyl acetate and extracted successively with sat. ammonium chloride solution, sat. sodium bisulfite solution, sat. sodium bicarbonate solution and sat. sodium chloride solution. The organic phase is dried over magnesium sulfate, filtered and concentrated under reduced pressure Chromatographic purification on silica gel (n-heptane/ethyl acetate 60/40) gives 5-chloro-2-fluoro-2-methanesulfonyl-1-methylindan-1-ol of melting point 148° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06670401B2 |
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| Source dataset | uspto-grants-2003_12 |
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| ORD ID | ord-3139c387bd7e4d2186b19a73bd0adb6e |
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| Source note | uspto-grants-2003_12 |
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