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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantBromineHCID 24408—
ReactantSodium ThiosulfateHCID 24477—
ReactantSodium hypobromiteHCID 23673712—
Reactant2-Acetyl-7-(allyloxybutyloxy)fluoreneHCID 69251958—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product2-(4-Allyloxybutyloxy)fluorene-7-carboxylic acidHCID 69251204—

Reaction Conditions

Temperature40 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07381350B2
Source datasetuspto-grants-2008_06
ORD IDord-67b74d1e3ba74f68a853bd1f9deaec5b
Source noteuspto-grants-2008_06