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Sodium hydride → HCID 86664596、化合物

HRID 1187776
ノート
印刷プレビュー

反応式

HRID 1187776 の反応式
[H-].[Na+].[Br:3][C:4]1[CH:5]=[CH:6][C:7]([CH:10]([OH:15])[C:11]([F:14])([F:13])[F:12])=[N:8][CH:9]=1.[F:16][C:17]([F:23])([F:22])[S:18](Cl)(=[O:20])=[O:19]>C(OCC)C>[Br:3][C:4]1[CH:5]=[CH:6][C:7]([CH:10]([O:15][S:18]([C:17]([F:23])([F:22])[F:16])(=[O:20])=[O:19])[C:11]([F:12])([F:13])[F:14])=[N:8][CH:9]=1
参加物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 24758Sodium hydrideHCID 79000Trifluoromethanesulfonyl chlorideHCID 672947601-(5-Bromopyridin-2-yl)-2,2,2-trifluoroethan-1-ol

生成物 1

HCID 86664596HCID 86664596、化合物収率 78%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒2 回

実験手順

To a stirred suspension of sodium hydride (765 mg, 60% dispersion in mineral oil) in dry diethyl ether (20 ml) under an argon atmosphere at 0° C. was added dropwise a solution of (RS)-1-(5-bromo-pyridin-2-yl)-2,2,2-trifluoro-ethanol (3.06 g) in diethyl ether (10 ml) and the resulting mixture was stirred at room temperature for 30 min. Trifluoromethanesulfonyl chloride (1.4 ml) was added and stirring was continued for a further 15 min at room temperature. The reaction mixture was quenched by addition of 10% aq. sodium bicarbonate solution and the mixture was extracted with diethyl ether. The phases were separated and the organic phase was washed with saturated brine. The organic phase was separated, dried over sodium sulphate, and concentrated in vacuo. The reside was purified by Kugelrohr distillation (60° C. oven temperature, 0.3 mbar) to give (RS)-trifluoro-methanesulfonic acid 1-(5-bromo-pyridin-2-yl)-2,2,2-trifluoro-ethyl ester (3.6 g, 78%) as a white solid. MS (EI): 389 ([{81Br}M]+), 387 ([{79Br}M]+), 320 ([{81Br}M−CF3]+), 318 ([{79Br}M−CF3]+), 256 ([{81Br}M−CF3—SO2]+), 254 ([{79Br}M−CF3—SO2]+), 240 ([{81Br}M−OSO2CF3]+), 238 ([{79Br}M−OSO2CF3]+).

後処理

  1. stirringstirring
  2. waitwas continued for a further 15 min at room temperature
  3. customThe reaction mixture was quenched by addition of 10% aq. sodium bicarbonate solution
  4. extractionthe mixture was extracted with diethyl ether
  5. customThe phases were separated
  6. washthe organic phase was washed with saturated brine
  7. customThe organic phase was separated
  8. dry with materialdried over sodium sulphate
  9. concentrationconcentrated in vacuo
  10. distillationThe reside was purified by Kugelrohr distillation (60° C. oven temperature, 0.3 mbar)

出典と根拠

ORDレコード
ord-96b09e6b97fa40ee8f891965c5d9d2d8
出典データセット
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08673950B2

反応ノート

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