HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22140Generated: October 25, 2026
2-Fluorobenzoyl chloride → 2-Di-n-propylamino-8-(2'-fluorobenzoyl)-1,2,3,4-tetrahydronaphthalene
https://huagongshe.com/reaction/22140
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Fluorobenzoyl chloride | HCID 9808 | — |
| Reactant | 8-Bromo-2-dipropylamino-1,2,3,4-tetrahydronaphthalene | HCID 14529564 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Di-n-propylamino-8-(2'-fluorobenzoyl)-1,2,3,4-tetrahydronaphthalene | HCID 15233537 | 29.9% |
Reaction Steps
2-Di-n-propylamino-8-bromo-1,2,3,4-tetrahydronaphthalene (1.0 g; 3.22 mmol) dissolved in THF (25 ml) was cooled to -78° C., and 2.5 ml of n-butyllithium (1.27M in hexane) were added. After one hour, o-fluorobenzoyl chloride (0.38 ml, 3.22 mmol) was added. The mixture was stirred for 10 minutes at -78° C. after which the reaction was quenched by addition of water at -78° C. The reaction was made basic with NaOH and extracted three times with methylene chloride. The basic extract was dried (Na2SO4) and concentrated to give 2.0 g of crude residue. Purification of this material by flash silica gel chromatography using 1:1 ether:hexane containing a trace of ammonium hydroxide as solvent provided 2-di-n-propylamino-8-(2'-fluorobenzoyl)-1,2,3,4-tetrahydronaphthalene (340 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05426226 |
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| Source dataset | uspto-grants-1995_06 |
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| ORD ID | ord-f1ba75c926ff440c8afffe4ef918c5b7 |
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| Source note | uspto-grants-1995_06 |
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