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Tetramethylammonium fluoride → HCID 67060889, 화합물

HRID 1623984
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HRID 1623984 반응식
[CH3:1][C:2]([S:5]([N:7]=[C:8]1[CH2:11][O:10][CH2:9]1)=[O:6])([CH3:4])[CH3:3].[F-].C[N+](C)(C)C.C[Si](C)(C)[C:20]([F:23])([F:22])[F:21]>C1COCC1>[CH3:4][C:2]([S:5]([NH:7][C:8]1([C:20]([F:23])([F:22])[F:21])[CH2:11][O:10][CH2:9]1)=[O:6])([CH3:1])[CH3:3]
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참가 물질

5

반응물 3

HCID 67803Tetramethylammonium fluorideHCID 552549(Trifluoromethyl)trimethylsilaneHCID 468399952-Methyl-N-(oxetan-3-ylidene)propane-2-sulfinamide

생성물 1

HCID 67060889HCID 67060889, 화합물수율 37.8%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

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온도
-35 °C

실험 절차

2-Methyl-N-(oxetan-3-ylidene)propane-2-sulfinamide (100 mg, 0.571 mmol) was dissolved in THF (2 mL). The solution was cooled down to −35° C. and added tetramethylammonium fluoride (63.8 mg, 0.685 mmol). The mixture was degassed and charged with argon. Trimethyl(trifluoromethyl)silane (0.134 ml, 0.856 mmol) in THF (1 mL) was added slowly via syringe. The reaction was stirred at this temperature for 2 h, warmed to −10° C. and quenched with saturated aqueous NH4Cl solution. The mixture was extracted with ethyl acetate, dried over anhydrous Na2SO4, and concentrated. The residue was purified by column chromatography to give the title compound (53 mg). LCMS m/z=246.2 [M+H]+; 1H NMR (400 MHz, CDCl3) δ 1.29 (s, 9H), 3.79 (s, 1H), 4.78-4.85 (m, 3H), 4.98 (dd, J=7.6 and 1.3 Hz, 1H).

후처리

  1. customThe mixture was degassed
  2. additioncharged with argon
  3. temperaturewarmed to −10° C.
  4. customquenched with saturated aqueous NH4Cl solution
  5. extractionThe mixture was extracted with ethyl acetate
  6. dry with materialdried over anhydrous Na2SO4
  7. concentrationconcentrated
  8. customThe residue was purified by column chromatography

출처 및 근거

ORD 기록
ord-7ad1d1d800eb4e8e90521a38162110bc
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08778950B2

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