Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 263636생성일: 2026년 10월 26일
Ethanol → 5-Fluoro-2-methyl-1-((4-(methylsulfinyl)phenyl)methylene)-1H-indene-3-acetic acid
https://huagongshe.com/reaction/263636
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Ethanol | HCID 702 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | N-[5-fluoro-2-methyl-1-(rho-methylsulfinylbenzylidene)-3-indenylacetyl]-glycine | HCID 70150105 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 5-Fluoro-2-methyl-1-((4-(methylsulfinyl)phenyl)methylene)-1H-indene-3-acetic acid | HCID 5352 | — |
반응 단계
N-[5-fluoro-2-methyl-1-(ρ-methylsulfinylbenzylidene)-3-indenylacetyl]-glycine. Benzyle-N-[5-fluoro-2-methyl-1-(ρ-methylsulfinylbenzylidene)-3-indenylacetyl]-glycinate (0.03 mole) in a mixture of 25 ml. of anhydrous ethanol and 2.5 ml. of 1N sodium hydroxide is allowed to stand at room temperature for 18 hours. The solution is diluted with water and extracted with ether. The aqueous layer is acidified with dilute hydrochloric acid and the organic product is extracted with ethyl acetate, washed with water and dried over sodium sulfate. Evaporation of the solution gives N-[5-fluoro-2-methyl-1-(ρ-methylsulfinylbenzylidene)-3-indenylacetic acid, the corresponding indenyl acyl glycine is obtained, which can be converted to the corresponding sulfonyl derivative using the procedure of Example 1E.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05643959 |
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| 출처 데이터셋 | uspto-grants-1997_07 |
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| ORD ID | ord-9f9891949e254cae9262f5b80d86bcca |
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| 출처 메모 | uspto-grants-1997_07 |
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