Potassium Hydroxide → 5-Methyl-4-pent-4-ynyl-2-phenyl-oxazole

HRID 2121697ノート

反応式

HRID 2121697 の反応式
[CH3:1][C:2]1[O:6][C:5]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)=[N:4][C:3]=1[CH2:13][CH2:14][CH2:15][C:16]#[C:17][Si](C)(C)C.[OH-].[K+]>CO>[CH3:1][C:2]1[O:6][C:5]([C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=2)=[N:4][C:3]=1[CH2:13][CH2:14][CH2:15][C:16]#[CH:17]

参加物

4

反応物 2

HCID 14797Potassium HydroxideHCID 120932675-Methyl-2-phenyl-4-(5-trimethylsilanyl-pent-4-ynyl)-oxazole

生成物 1

HCID 120932685-Methyl-4-pent-4-ynyl-2-phenyl-oxazole

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

Alkyne 1-6 (1.9 g, 6.3 mmol) was dissolved in methanol (100 mL) at 23° C. under N2 atmosphere. An aqueous solution of 10% KOH (10 mL) was then added and the reaction stirred for 12 hours. Solvent removed in vacuo and residue partitioned between ethyl acetate (200 mL) and water (200 mL). The organic layer was washed with water, brine and dried over MgSO4. The crude product 1-7 was used in the following step without further purification.

後処理

  1. customSolvent removed in vacuo and residue
  2. custompartitioned between ethyl acetate (200 mL) and water (200 mL)
  3. washThe organic layer was washed with water, brine
  4. dry with materialdried over MgSO4
  5. customThe crude product 1-7 was used in the following step without further purification

出典と根拠

ORDレコード
ord-e6b2a070d385485b864fb9bca2e12a26
出典データセット
uspto-grants-2004_02
特許番号
US06696474B2

反応ノート

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