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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Dicyclohexylcarbodiimide → 428452-46-4

HRID 2415644
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HRID 2415644 반응식
[F:1][C:2]([F:10])([CH2:6][C:7]([OH:9])=[O:8])[C:3]([OH:5])=[O:4].[CH:11]1(N=C=NC2CCCCC2)CCCCC1>C1COCC1>[CH3:11][O:4][C:3](=[O:5])[C:2]([F:10])([F:1])[CH2:6][C:7]([OH:9])=[O:8]
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참가 물질

4

반응물 2

HCID 10868DicyclohexylcarbodiimideHCID 695812,2-Difluorosuccinic acid

생성물 1

HCID 13935575428452-46-4수율 77.9%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Commercially available 2,2-difluorosuccinic acid (8.0 g, 51.9 mmol) was dissolved in THF and cooled on ice before addition of 1,3-dicyclohexylcarbodiimide (11.8 g, 57.2 mmol). The mixture was stirred at room temperature for 3 hours, cooled and filtered. The filtrate was concentrated in vacuo. The residue was stirred with methanol (50 ml) for 3 hours at room temperature and then solvents were removed in vacuo to afford the crude ester as an oil (8.4 g). The oil was purified by column chromatography on silica gel column and elution with a 0-100% ethyl acetate/toluene gradient to afford 2,2-difluorosuccinic acid 1-methyl ester as a colorless oil (6.8 g).

후처리

  1. temperaturecooled
  2. filtrationfiltered
  3. concentrationThe filtrate was concentrated in vacuo
  4. stirringThe residue was stirred with methanol (50 ml) for 3 hours at room temperature
  5. customsolvents were removed in vacuo
  6. customto afford the crude ester as an oil (8.4 g)
  7. customThe oil was purified by column chromatography on silica gel column and elution with a 0-100% ethyl acetate/toluene gradient

출처 및 근거

ORD 기록
ord-cd6f12bc4f3f45308e5b34d9da9ad1b1
출처 데이터셋
uspto-grants-2004_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06821960B2

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