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Hydrochloric Acid → 2-Ethylthiomethyl-4-methylpentanoic acid

HRID 374701
ノート
印刷プレビュー

反応式

HRID 374701 の反応式
[CH2:1]([S:3][CH2:4][CH:5]([CH2:11][CH:12]([CH3:14])[CH3:13])[C:6]([O:8]CC)=[O:7])[CH3:2].O.Cl>C(OCC)(=O)C.C(O)C.[OH-].[K+]>[CH2:1]([S:3][CH2:4][CH:5]([CH2:11][CH:12]([CH3:13])[CH3:14])[C:6]([OH:8])=[O:7])[CH3:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 313Hydrochloric AcidHCID 962WaterHCID 22418875Ethyl 2-ethylthiomethyl-4-methylpentanoate

生成物 1

HCID 224189692-Ethylthiomethyl-4-methylpentanoic acid収率 101.9%

試薬・触媒・溶媒 2

HCID 14797Potassium Hydroxide溶媒HCID 21584252Ethanol ethylacetate
溶媒
2 回

実験手順

650 mg of ethyl 2-ethylthiomethyl-4-methylpentanoate was dissolved in 6 ml of an ethanol/water (10/1) solution, 8.9 ml of an ethanol/water (10/1) solution of 2N potassium hydroxide was added thereto. The solution was stirred at room temperature for 2.5 hours, and then, the reaction solution was distilled off under reduced pressure to obtain a suspension. To this suspension, 40 ml of water was added, and the reaction solution was adjusted to pH2 with 2N hydrochloric acid under cooling with ice, and extracted with ethyl acetate. The ethyl acetate layer was washed with water and then with a saturated sodium chloride aqueous solution and dried over anhydrous sodium sulfate. Then, the solvent was distilled off to obtain 577 mg of 2-ethylthiomethyl-4-methylpentanoic acid as colorless oily substance.

後処理

  1. additionwas added
  2. distillationthe reaction solution was distilled off under reduced pressure
  3. customto obtain a suspension
  4. temperatureunder cooling with ice
  5. extractionextracted with ethyl acetate
  6. washThe ethyl acetate layer was washed with water
  7. dry with materialwith a saturated sodium chloride aqueous solution and dried over anhydrous sodium sulfate
  8. distillationThen, the solvent was distilled off

出典と根拠

ORDレコード
ord-e65400975a3d4dbd92f9d2b761b23ad9
出典データセット
uspto-grants-1996_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05481036

反応ノート

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