Sodium Hydroxide → 4-Methyl-2-(4-methylphenyl)-1,3-thiazole-5-carboxylic acid

HRID 58549

反応式

HRID 58549 の反応式
[CH3:1][C:2]1[N:3]=[C:4]([C:12]2[CH:17]=[CH:16][C:15]([CH3:18])=[CH:14][CH:13]=2)[S:5][C:6]=1[C:7]([O:9]CC)=[O:8].[OH-].[Na+]>O.C(O)C>[CH3:1][C:2]1[N:3]=[C:4]([C:12]2[CH:17]=[CH:16][C:15]([CH3:18])=[CH:14][CH:13]=2)[S:5][C:6]=1[C:7]([OH:9])=[O:8]

参加物

5

反応物 2

HCID 14798Sodium HydroxideHCID 3776504Ethyl 4-Methyl-2-(4-methylphenyl)thiazole-5-carboxylate

生成物 1

HCID 27636254-Methyl-2-(4-methylphenyl)-1,3-thiazole-5-carboxylic acid収率 88%

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 962Water溶媒

実験手順

The mixture of ethyl 4-methyl-2-p-tolylthiazole-5-carboxylate (0.200 g; 0.765 mmol) and sodium hydroxide (0.0643 g; 1.61 mmol) in water (4 mL) and ethanol (8 mL) was irradiated in a microwave oven at 130° C. for 5 min. The mixture was concentrated (removal of ethanol), and the pH of the solution was adjusted to 3 by addition of 6N hydrochloric acid. The acidic solution was extracted with (3×10 mL) of ethyl acetate. Combined organic layers were dried over magnesium sulfate, and evaporated to afford 0.157 g (88%) of 4-methyl-2-p-tolylthiazole-5-carboxylic acid as a white solid which was directly used in the next step.

後処理

  1. customwas irradiated in a microwave oven at 130° C. for 5 min
  2. concentrationThe mixture was concentrated
  3. custom(removal of ethanol)
  4. additionthe pH of the solution was adjusted to 3 by addition of 6N hydrochloric acid
  5. extractionThe acidic solution was extracted with (3×10 mL) of ethyl acetate
  6. dry with materialCombined organic layers were dried over magnesium sulfate
  7. customevaporated

出典と根拠

ORDレコード
ord-662b1f28457244c698aeed22675af644
出典データセット
uspto-grants-2016_09
特許番号
US09434722B2

関連ノート

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