HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1077304Generated: November 1, 2026
Hydrochloric Acid → 1-(7-Ethyl-9H-fluoren-2-YL)ethan-1-one
https://huagongshe.com/reaction/1077304
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2-Ethyl-9H-fluorene | HCID 274939 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | 1-(7-Ethyl-9H-fluoren-2-YL)ethan-1-one | HCID 21503908 | — |
Reaction Steps
Acetic anhydride (2.67 g.) in dichloroethane (10 ml.) was added dropwise to a stirred, cooled (0°) suspension of aluminum chloride (6.95 g.) in dichloroethane (20 ml.). Cooling and stirring were continued during the dropwise addition of a solution of 2-ethylfluorene (4.61 g.) in dichloroethane (50 ml.). The mixture was stirred for one hour at room temperature and then decomposed by the dropwise addition of 2N-hydrochloric acid (40 ml.) to the cooled solution. The organic layer was separated, washed with water and with aqueous sodium bicarbonate, dried over anhydrous sodium sulphate, filtered, and evaporated under reduced pressure. The residue was recrystallised from light petroleum (ca 250 ml., b.p. 60°-80°) to give 2-acetyl-7-ethylfluorene m.p. 120°-122°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03959482 |
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| Source dataset | uspto-grants-1976_05 |
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| ORD ID | ord-9e60e01118f34d20b67d204e025b32b2 |
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| Source note | uspto-grants-1976_05 |
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