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Hydrochloric Acid → 2-Ethylthiomethyl-4-methylpentanoic acid

HRID 1720667
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HRID 1720667 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

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

생성물 1

HCID 224189692-Ethylthiomethyl-4-methylpentanoic acid수율 101.9%

시약·촉매·용매 2

HCID 14797Potassium Hydroxide용매HCID 21584252Ethanol ethylacetate
용매
2회

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-b152870404064bb8921f49b6eb845ba7
출처 데이터셋
uspto-grants-1996_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05506356

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