HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656808Generated: October 29, 2026
Diisopropylamine → 2-Fluoro-2-methyl-1-tetralone
https://huagongshe.com/reaction/1656808
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | 2-Methyl-1-tetralone | HCID 102650 | — |
| Reactant | N-Fluorobenzenesulfonimide | HCID 588007 | — |
| Reactant | Lithium diisopropylamine | HCID 45051747 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Fluoro-2-methyl-1-tetralone | HCID 15014456 | 50% |
Reaction Steps
0.16 milliliter diisopropylamine in 10 milliliters tetrahydrofuran were allowed to stand with 1.15 equivalents butyllithium at -25° C. The resulting solution of lithium diisopropylamine was cooled to -78° C. and 1 equivalent 2-methyl-1-tetralone in 5 milliliters tetrahydrofuran solution was dropped in. The mixture was allowed to stand at -70° C. for 100 minutes. 1.5 equivalents N-fluorobenzenesulfonimide prepared according to Example 1 above in 11 milliliters tetrahydrofuran were mixed rapidly with the mixture at -95° C. The mixture was quenched with 30 milliliters ammonium chloride solution and extracted with dichloromethane. The organic phase was dried with magnesium sulfate, filtered, and evaporated. 2-methyl-2-fluoro-tetralone was obtained in 50% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05254732 |
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| Source dataset | uspto-grants-1993_10 |
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| ORD ID | ord-225051308dab4752838f27b03d9e6062 |
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| Source note | uspto-grants-1993_10 |
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