HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 130274Erstellt: 24. Oktober 2026
Hydrochloric Acid → 2-(4-Allyloxybutyloxy)fluorene-7-carboxylic acid
https://huagongshe.com/de/reaction/130274
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Bromine | HCID 24408 | — |
| Edukt | Sodium Thiosulfate | HCID 24477 | — |
| Edukt | Sodium hypobromite | HCID 23673712 | — |
| Edukt | 2-Acetyl-7-(allyloxybutyloxy)fluorene | HCID 69251958 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | 2-(4-Allyloxybutyloxy)fluorene-7-carboxylic acid | HCID 69251204 | — |
Reaktionsschritte
A dioxane (380 ml) solution of 2-acetyl-7-(4-allyloxybutyloxy)fluorene 22 g was cooled to 8° C. Sodium hypobromite prepared from water 209 ml, sodium hydroxide 42.7 g and bromine 15.2 ml was dropwise added thereto, and after finishing dropwise adding, the solution was stirred at 40° C. for 15 minutes. The reaction mixture was cooled to 10° C., and then a saturated sodium thiosulfate aqueous solution was added thereto. A solid matter deposited by acidifying the solution with hydrochloric acid was filtered and then dried. The solid matter was recrystallized from acetic acid to obtain 15 g of 2-(4-allyloxybutyloxy)fluorene-7-carboxylic acid. Phase transition temperature: C164N222I.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07381350B2 |
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| Quelldatensatz | uspto-grants-2008_06 |
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| ORD ID | ord-67b74d1e3ba74f68a853bd1f9deaec5b |
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| Quellennotiz | uspto-grants-2008_06 |
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