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Hydrochloric Acid → 4-Methyl-2-sulfanylbenzoic acid

HRID 539951
ノート
印刷プレビュー

反応式

HRID 539951 の反応式
CN(C)C([S:5][C:6]1[CH:15]=[C:14]([CH3:16])[CH:13]=[CH:12][C:7]=1[C:8]([O:10]C)=[O:9])=O.Cl>[OH-].[Na+]>[CH3:16][C:14]1[CH:13]=[CH:12][C:7]([C:8]([OH:10])=[O:9])=[C:6]([SH:5])[CH:15]=1
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

4

反応物 2

HCID 313Hydrochloric AcidHCID 21761355Methyl 2-[(dimethylcarbamoyl)sulfanyl]-4-methylbenzoate

生成物 1

HCID 200954184-Methyl-2-sulfanylbenzoic acid

試薬・触媒・溶媒 1

HCID 14798Sodium Hydroxide溶媒

反応条件

温度
0 °C

実験手順

A round bottle flask containing a mixture of methyl 2-[(dimethylcarbamoyl)sulfanyl]-4-methylbenzoate (50 g, 197.6 mmol) and an aqueous solution of sodium hydroxide (120 mL, 4 N) was vacuumed and backfilled with nitrogen 3 times. After being refluxed for 2 hours, the resulting mixture was cooled to 0° C. and acidified with an aqueous solution of hydrochloric acid (45 mL, 6 N). The formed precipitate was collected by filtration, and then dissolved in ethyl acetate (500 mL). The solution was dried over anhydrous sodium sulfate, and concentrated in vacuo to afford 4-methyl-2-sulfanylbenzoic acid as a light yellow solid.

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート

後処理

  1. additionA round bottle flask containing
  2. temperatureAfter being refluxed for 2 hours
  3. filtrationThe formed precipitate was collected by filtration
  4. dissolutiondissolved in ethyl acetate (500 mL)
  5. dry with materialThe solution was dried over anhydrous sodium sulfate
  6. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-5870ec31c9344498bc9543a92cbe5025
出典データセット
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08871756B2

反応ノート

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