HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650192Generated: October 31, 2026
Hexane → 4-(1-Naphthoyl)-3,5-dichlorotoluene
https://huagongshe.com/reaction/1650192
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 3,5-Dichlorotoluene | HCID 32834 | — |
| Reactant | 1-Naphthalenecarbonyl chloride | HCID 70146 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Butyllithium | HCID 178418339 | — |
| Product | 4-(1-Naphthoyl)-3,5-dichlorotoluene | HCID 14700029 | 104.1% |
Reaction Steps
To a stirred, cold (-60° C.) solution of 3,5-dichlorotoluene (3.5 g, 21.7 mmol) in dry tetrahydrofuran (30 ml), 2.6 M n-butyllithium in hexane (8.78 ml, 22.8 mmol) was added dropwise over 15 minutes. The reaction mixture was stirred for one hour at -60° C. and then treated with a solution of 1-naphthoyl chloride (4.14 g, 21.7 mmol) in 15 ml of dry tetrahydrofuran over a period of 15 minutes. The mixture was stirred for 3.5 hours at -60° C. and then quenched with 4.8 ml of saturated NH4Cl solution. The mixture was permitted to warm to room temperature and then diluted with 30 ml of water and 30 ml of ether. The layers were thoroughly mixed and then separated. The etheral layer was backed-washed with brine and dried with anhydrous magnesium sulfate. Concentration afforded 7.12 g of crude product which was chromatographed on silica gel (20:1 hexane:ethyl acetate) to give 1.59 g (23 %).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04923885 |
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| Source dataset | uspto-grants-1990_05 |
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| ORD ID | ord-f97f253af5084068965eced3708b300f |
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| Source note | uspto-grants-1990_05 |
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