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Ammonia → 4-Morpholinecarbothioamide

HRID 53936
ノート
印刷プレビュー

反応式

HRID 53936 の反応式
[C:1](C1NC=CN=1)(C1NC=CN=1)=[S:2].[NH:13]1[CH2:18][CH2:17][O:16][CH2:15][CH2:14]1.[NH3:19]>C1COCC1>[NH2:19][C:1]([N:13]1[CH2:18][CH2:17][O:16][CH2:15][CH2:14]1)=[S:2]
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 222AmmoniaHCID 8083Morpholine2 回HCID 11412697Thiocarbonyl diimidazole

生成物 1

HCID 23935444-Morpholinecarbothioamide収率 76%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

A solution of 3.35 g (18.8 mmol) of thiocarbonyl diimidazole in 100 ml of THF was treated with 0.82 ml (9.4 mmol) of morpholine. After being stirred at ambient temperature for 3.5 h, an additional 0.82 ml portion of morpholine was added, and stirring was continued. After 6 h, the solution was treated with excess concentrated aqueous ammonia, and stirred overnight. The resulting solution was concentrated in vacuo, taken up in chloroform, separated from the aqueous phase, dried over Na2SO4, and concentrated. Purification of the residue by silica gel chromatography using ethyl acetate provided 1.85 g (76%) of the desired compound, Rf 0.17 (10% methanol in chloroform), as a white solid. 1H NMR (CDCl3) δ 3.76 (m, 4 H), 3.83 (m, 4 H), 5.75 (br, 2 H). Mass spectrum: (M+H)+ =147.

後処理

  1. stirringstirring
  2. waitAfter 6 h
  3. stirringstirred overnight
  4. concentrationThe resulting solution was concentrated in vacuo
  5. customseparated from the aqueous phase
  6. dry with materialdried over Na2SO4
  7. concentrationconcentrated
  8. customPurification of the residue by silica gel chromatography

出典と根拠

ORDレコード
ord-37c5fddb6eed44179c3fbb7830da8477
出典データセット
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05621109

反応ノート

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