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Hydrochloric Acid → 4-(Cyclopentyloxy)-3-methoxybenzoic acid

HRID 2230989
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HRID 2230989 반응식
[CH:1]1([O:6][C:7]2[CH:17]=[CH:16][C:10]([C:11]([O:13]CC)=[O:12])=[CH:9][C:8]=2[O:18][CH3:19])[CH2:5][CH2:4][CH2:3][CH2:2]1.[OH-].[Na+].Cl>C(O)C.O1CCOCC1>[CH:1]1([O:6][C:7]2[CH:17]=[CH:16][C:10]([C:11]([OH:13])=[O:12])=[CH:9][C:8]=2[O:18][CH3:19])[CH2:2][CH2:3][CH2:4][CH2:5]1
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참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 22724204Ethyl 4-cyclopentyloxy-3-methoxybenzoate

생성물 1

HCID 227243044-(Cyclopentyloxy)-3-methoxybenzoic acid수율 77%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 312751,4-Dioxane용매

반응 조건

온도
80 °C

실험 절차

A mixture of ethyl 4-cyclopentyloxy-3-methoxybenzoate (1.06 g) and 4N aqueous sodium hydroxide (4 ml) in ethanol (8 ml) and 1,4-dioxane (8 ml) was stirred at 80° C. for 3 hours. Then the mixture was poured into dilute hydrochloric acid and extracted with ethyl acetate. The organic solution was washed with dilute hydrochloric acid and brine, dried over magnesium sulfate and concentrated. The resultant solid was collected and washed with isopropyl ether to give 4-cyclopentyloxy-3-methoxybenzoic acid (730 mg).

후처리

  1. extractionextracted with ethyl acetate
  2. washThe organic solution was washed with dilute hydrochloric acid and brine
  3. dry with materialdried over magnesium sulfate
  4. concentrationconcentrated
  5. customThe resultant solid was collected
  6. washwashed with isopropyl ether

출처 및 근거

ORD 기록
ord-bb7d17f58239468abf7ba1afaf02262b
출처 데이터셋
uspto-grants-2002_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06426345B1

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