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Hydrochloric Acid → Piperic acid

HRID 631938
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HRID 631938 반응식
[CH:1]1[C:6](/[CH:7]=[CH:8]/[CH:9]=[CH:10]/[C:11](N2CCCCC2)=[O:12])=[CH:5][C:4]2[O:19][CH2:20][O:21][C:3]=2[CH:2]=1.[OH-:22].[K+].Cl>C(O)C>[O:21]1[C:3]2[CH:2]=[CH:1][C:6](/[CH:7]=[CH:8]/[CH:9]=[CH:10]/[C:11]([OH:12])=[O:22])=[CH:5][C:4]=2[O:19][CH2:20]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 14797Potassium HydroxideHCID 638024Piperine

생성물 1

HCID 5370536Piperic acid수율 79.2%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Piperine (200 mg, 0.70 mmol) dissolved in anhydrous ethanol and KOH (1.18 g, 21.0 mmol) were mixed and heated to reflux for 12 hours. Upon completion of the experiment, the pH value of the reaction mixture solution was adjusted to 2-3 using hydrochloric acid. After the ethanol was distilled under reduced pressure, the residue was diluted with EtOAC (30 mL) and washed with a saturated solution of NaCl, followed by drying over anhydrous Na2SO4. The solvent was distilled under reduced pressure to give a target compound (121 mg, yield: 79.1%).

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후처리

  1. temperatureheated
  2. temperatureto reflux for 12 hours
  3. distillationAfter the ethanol was distilled under reduced pressure
  4. additionthe residue was diluted with EtOAC (30 mL)
  5. washwashed with a saturated solution of NaCl
  6. dry with materialby drying over anhydrous Na2SO4
  7. distillationThe solvent was distilled under reduced pressure

출처 및 근거

ORD 기록
ord-87436eee3392488f87d68225bb8e11aa
출처 데이터셋
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09321751B2

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