HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890372Generated: October 31, 2026
Ethylene → 6-Fluoro-1,2,3,4-tetrahydronaphthalen-2-one
https://huagongshe.com/reaction/890372
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylene | HCID 6325 | — |
| Reactant | 2-(4-Fluorophenyl)acetic acid | HCID 9837 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | 6-Fluoro-1,2,3,4-tetrahydronaphthalen-2-one | HCID 5044385 | — |
Reaction Steps
4-fluorophenylacetic acid (1 equivalent) was dissolved in dichloroethane (1.3 M) containing SOCl2 (3 equivalents), the mixture was refluxed for 90 minutes and the solvent was removed. Solution of this crude product in CH2Cl2 was added dropwise within 60 minutes to AlCl3 (2 eq) in CH2Cl2 (0.4 M) while stirring at 0° C. Thereafter, ethylene was introduced at 0° C. over 45 minutes, whereupon the mixture was stirred further at room temperature for 1 hour, and thereafter was treated at 0° C. with ice-water. The organic phase was washed with 1 N HCl (2×), NaHCO3 (sat. sol.), dried and evaporated. The residue was triturated with hexane, yielding the product as a bright yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06995269B2 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-9b53831fa1fb4b54ae682bbb1bfc52a3 |
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| Source note | uspto-grants-2006_02 |
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