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Trifluoroacetic anhydride → HCID 86087049, 화합물

HRID 1992989
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HRID 1992989 반응식
[CH3:1][C:2]1[C:3](=O)[C:4]([O:10][CH3:11])([O:8][CH3:9])[C:5]=1[O:6]C.[CH3:13][O:14][C:15]1[CH:16]=[C:17]([Mg]Br)[CH:18]=[CH:19][CH:20]=1.C(OC(C(F)(F)F)=O)(C(F)(F)F)=O>C1COCC1>[CH3:1][C:2]1[C:5](=[O:6])[C:4]([O:10][CH3:11])([O:8][CH3:9])[C:3]=1[C:19]1[CH:18]=[CH:17][CH:16]=[C:15]([O:14][CH3:13])[CH:20]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 9845Trifluoroacetic anhydrideHCID 103972413,4,4-trimethoxy-2-methylcyclobut-2-en-1-oneHCID 178490745HCID 178490745, 화합물

생성물 1

HCID 86087049HCID 86087049, 화합물수율 75%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A THF solution (12 mL) of known 2-methyl-3,4,4-tris(methyloxy)-2-cyclobuten-1-one (0.500 g, 2.91 mmol, 1 equiv) was cooled to ca. −78° C. 3-Methoxyphenyl magnesium bromide (4.36 mL, 1.0 M, 1.5 equiv) was added. After 5 min, TFAA (0.657 mL, 4.66 mmol, 1.6 equiv) was added. The reaction was quenched with saturated NaHCO3 (5 mL) after an additional 5 min. Extraction with EtOAc was followed by drying (Na2SO4), filtration, and concentration to a bright yellow oil. Radial chromatography (SiO2, 4 mm plate, 80:20; hexanes/EtOAc) afforded the title compound (245) as a bright yellow oil (0.540 g, 75%). 1H NMR (CDCl3, 300 MHz) δ 7.44-7.33 (m, 3H), 7.15-7.09 (m, 1H), 3.89 (s, 3H), 3.54 (s, 6H), 2.13 (s, 3H). TLC (60:40; hexanes/EtOAc): Rf=0.45.

후처리

  1. customThe reaction was quenched with saturated NaHCO3 (5 mL) after an additional 5 min
  2. extractionExtraction with EtOAc
  3. customby drying
  4. filtration(Na2SO4), filtration, and concentration to a bright yellow oil

출처 및 근거

ORD 기록
ord-cb37c194de3843348ff493cc1f82c484
출처 데이터셋
uspto-grants-2010_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07649093B2

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