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Tetramethylammonium fluoride → HCID 67060889、化合物

HRID 1623984
ノート
印刷プレビュー

反応式

HRID 1623984 の反応式
[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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

HCID 67060889HCID 67060889、化合物収率 37.8%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
-35 °C

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-7ad1d1d800eb4e8e90521a38162110bc
出典データセット
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08778950B2

反応ノート

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