반응 #217456

ord-67b74d1e3ba74f68a853bd1f9deaec5b

반응 방정식

Cl
hydrochloric acid
C=CCOCCCCOc1ccc2c(c1)Cc1cc(C(C)=O)ccc1-2
2-acetyl-7-(4-allyloxybutyloxy)fluorene
[Na+].[O-]Br
Sodium hypobromite
[Na+].[OH-]
sodium hydroxide
BrBr
bromine
O=S([O-])([O-])=S.[Na+].[Na+]
sodium thiosulfate
C=CCOCCCCOc1ccc2c(c1)Cc1cc(C(=O)O)ccc1-2
2-(4-allyloxybutyloxy)fluorene-7-carboxylic acid

반응 조건

온도
40°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONwas dropwise added
  2. 2
    workup.ADDITIONafter finishing dropwise adding
  3. 3
    온도The reaction mixture was cooled to 10° C.
  4. 4
    여과was filtered
  5. 5
    기타dried
  6. 6
    기타The solid matter was recrystallized from acetic acid

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07381350B2uspto-grants-2008_06