HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 130274Generated: October 26, 2026
Hydrochloric Acid → 2-(4-Allyloxybutyloxy)fluorene-7-carboxylic acid
https://huagongshe.com/reaction/130274
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Sodium hypobromite | HCID 23673712 | — |
| Reactant | 2-Acetyl-7-(allyloxybutyloxy)fluorene | HCID 69251958 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-(4-Allyloxybutyloxy)fluorene-7-carboxylic acid | HCID 69251204 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07381350B2 |
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| Source dataset | uspto-grants-2008_06 |
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| ORD ID | ord-67b74d1e3ba74f68a853bd1f9deaec5b |
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| Source note | uspto-grants-2008_06 |
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