참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Bromine | HCID 24408 | — |
| 반응물 | Sodium Thiosulfate | HCID 24477 | — |
| 반응물 | Sodium hypobromite | HCID 23673712 | — |
| 반응물 | 2-Acetyl-7-(allyloxybutyloxy)fluorene | HCID 69251958 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | 2-(4-Allyloxybutyloxy)fluorene-7-carboxylic acid | HCID 69251204 | — |
반응 단계
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 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US07381350B2 |
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| 출처 데이터셋 | uspto-grants-2008_06 |
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| ORD ID | ord-67b74d1e3ba74f68a853bd1f9deaec5b |
|---|
| 출처 메모 | uspto-grants-2008_06 |
|---|
