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Sodium Hydroxide → 2-(But-3-ynyl)-5-phenyloxazole

HRID 1189092
ノート
印刷プレビュー

反応式

HRID 1189092 の反応式
O=P12OP3(OP(OP(O3)(O1)=O)(=O)O2)=O.O=[C:16]([C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1)[CH2:17][NH:18][C:19](=[O:24])[CH2:20][CH2:21][C:22]#[CH:23].[OH-].[Na+]>O=P(Cl)(Cl)Cl>[CH2:20]([C:19]1[O:24][C:16]([C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)=[CH:17][N:18]=1)[CH2:21][C:22]#[CH:23]
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 14798Sodium Hydroxide2 回HCID 14812Phosphorus oxide (P4O10)HCID 86086916Pent-4-ynoic acid (2-oxo-2-phenyl-ethyl)-amide

生成物 1

HCID 860869172-(But-3-ynyl)-5-phenyloxazole収率 21.6%

試薬・触媒・溶媒 1

HCID 24813Phosphorus oxychloride溶媒

反応条件

温度
105 °C

実験手順

907 mg (6.39 mmol) of P2O5 were added to a solution of pent-4-ynoic acid (2-oxo-2-phenyl-ethyl)-amide (160 mg, 0.74 mmol) in POCl3 (10.4 mL). The reaction mixture was stirred for 2 hours at 105° C. and then poured carefully onto ice. The solution was basified with NaOH 1N followed by NaOH pellets till pH=8. The aqueous phase was extracted thrice with DCM. The organic phase was washed with brine, dried over MgSO4, filtered and evaporated. The crude residue was purified by flash chromatography (DCM/MeOH 99:1) to yield 31 mg (0.16 mmol, 21%) of 2-(but-3-ynyl)-5-phenyloxazole as an orange oil.

後処理

  1. additionpoured carefully onto ice
  2. extractionThe aqueous phase was extracted thrice with DCM
  3. washThe organic phase was washed with brine
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. customevaporated
  7. customThe crude residue was purified by flash chromatography (DCM/MeOH 99:1)

出典と根拠

ORDレコード
ord-23ad856262c64373a3554f2afd5ba9ea
出典データセット
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08674106B2

反応ノート

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