HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325863Generated: October 30, 2026
Hydrochloric Acid → HCID 10681666, compound
https://huagongshe.com/reaction/325863
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | HCID 20462999 | HCID 20462999 | — |
| Reactant | HCID 20463006 | HCID 20463006 | — |
| Reactant | 3-Bromo-6-fluoro-1-indanone | HCID 23293681 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 10681666 | HCID 10681666 | — |
Reaction Steps
In a corresponding manner was made 3-bromo-6-fluoro-1-indanone melting at 62-64 degrees Centigrade, and 3-bromo-5-fluoro-1-indanone melting at 44-47 degrees Centigrade. To a solution of 113 grams of 3-bromo-6-chloro-1-indanone in 1400 milliliters of dry benzene were added over 10 minutes 230 grams of aluminiumchloride in portions. The reaction mixture was then refluxed for 3 hours, cooled and treated with crushed ice and concentrated hydrochloric acid. The organic phase was separated and extracted with 1 N sodium hydroxide and water, dried over anhydrous magnesium sulfate, treated with active carbon and concentrated in vacuo. The residue was taken up to 450 milliliters of hot n-hexane, cooled and filtered to give 96 grams of 3-phenyl-6-chloro-1-indanone melting at 84-92 degrees Centigrade.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04443448 |
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| Source dataset | uspto-grants-1984_04 |
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| ORD ID | ord-cc5c5c0fa6dd4aeb9dfd49e9efac0dd4 |
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| Source note | uspto-grants-1984_04 |
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