Triethylamine → 1-Isoxazol-3-ylethyl methanesulfonate

HRID 1896645ノート

反応式

HRID 1896645 の反応式
[CH3:1][S:2]([O:5]S(C)(=O)=O)(=[O:4])=[O:3].[O:10]1[CH:14]=[CH:13][C:12]([CH:15](O)[CH3:16])=[N:11]1.C(N(CC)CC)C.C(OCC)(=O)C>C1COCC1>[CH3:1][S:2]([O:5][CH:15]([C:12]1[CH:13]=[CH:14][O:10][N:11]=1)[CH3:16])(=[O:4])=[O:3]

参加物

6

反応物 4

HCID 8471TriethylamineHCID 8857Ethyl AcetateHCID 81560Methanesulfonic anhydride2 回HCID 231647251-Isoxazol-3-ylethanol2 回

生成物 1

HCID 574617131-Isoxazol-3-ylethyl methanesulfonate

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

Methanesulfonic anhydride (825 mg, 4.74 mmol) was added to a solution of 1-isoxazol-3-ylethanol (C6 from the previous step, 536 mg) and triethylamine (0.90 mL, 6.5 mmol) in THF (10 mL), and the reaction mixture was stirred for 18 hours. After addition of ethyl acetate, the mixture was washed with water, dried over magnesium sulfate, filtered, and concentrated in vacuo. The reaction was judged to be incomplete by proton NMR spectroscopy, so this material was resubjected to the reaction conditions, using two equivalents of methanesulfonic anhydride, and worked up in the same manner. The crude material was purified by silica gel chromatography (Eluants: 25% ethyl acetate in heptane followed by 50% ethyl acetate in heptane) to provide the product as a colorless oil. Yield: 276 mg, 1.44 mmol, 14% over 2 steps. 1H NMR (400 MHz, CDCl3) δ 1.81 (d, J=6.6 Hz, 3H), 3.01 (s, 3H), 5.93 (q, J=6.6 Hz, 1H), 6.50 (d, J=1.8 Hz, 1H), 8.45 (d, J=1.7 Hz, 1H).

後処理

  1. washthe mixture was washed with water
  2. dry with materialdried over magnesium sulfate
  3. filtrationfiltered
  4. concentrationconcentrated in vacuo
  5. customwas resubjected to the reaction conditions
  6. customThe crude material was purified by silica gel chromatography (Eluants: 25% ethyl acetate in heptane followed by 50% ethyl acetate in heptane)

出典と根拠

ORDレコード
ord-a4673c8fd3f44383b5ce545f817ac868
出典データセット
uspto-grants-2013_08
特許番号
US08518944B2

反応ノート

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