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Ethanol → 1-(Carboxy)-1-(4-methoxybenzylthio)cyclohexane

HRID 375556
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HRID 375556 반응식
[C:1]([C:6]1([S:12][CH2:13][C:14]2[CH:19]=[CH:18][C:17]([O:20][CH3:21])=[CH:16][CH:15]=2)[CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]1)([O:3]CC)=[O:2].[OH-].[Na+].C(O)C.O.[OH-].[Li+]>O.O1CCCC1>[C:1]([C:6]1([S:12][CH2:13][C:14]2[CH:19]=[CH:18][C:17]([O:20][CH3:21])=[CH:16][CH:15]=2)[CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]1)([OH:3])=[O:2]
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HCID 702EthanolHCID 14798Sodium HydroxideHCID 168937Lithium hydroxide, monohydrateHCID 224002131-(Carboethoxy)-1-(4-methoxybenzylthio)cyclohexane

생성물 1

HCID 212169071-(Carboxy)-1-(4-methoxybenzylthio)cyclohexane수율 92%

시약·촉매·용매 2

HCID 962
Water
용매
HCID 8028Tetrahydrofuran용매

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온도
60 °C

실험 절차

Dissolve 1-(carboethoxy)-1-(4-methoxybenzylthio)cyclohexane (1.45 g, 4.7 mmol) in water (2.5 mL) and tetrahydrofuran (10 mL). Treat with 2.5N sodium hydroxide (4 mL, 10 mmol). Heat at 60° C. for 2 hours, add 95% ethanol (10 mL) and lithium hydroxide monohydrate (0.42 g, 10 mmol) Heat to a gentle reflux for 20 hours, cool and evaporate the solvent in vacuo. Partition between water (50 mL) and ether (50 mL). Separate the aqueous phase and acidify to pH 1. Extract with methylene chloride (50 mL), dry (Na2SO4) and evaporate the solvent in vacuo to give 1-(carboxy)-1-(4-methoxybenzylthio)cyclohexane as a white solid (1.21 g, 92%).

후처리

  1. temperatureHeat to
  2. temperaturea gentle reflux for 20 hours
  3. temperaturecool
  4. customevaporate the solvent in vacuo
  5. customPartition between water (50 mL) and ether (50 mL)
  6. customSeparate the aqueous phase
  7. extractionExtract with methylene chloride (50 mL)
  8. dry with materialdry (Na2SO4)
  9. customevaporate the solvent in vacuo

출처 및 근거

ORD 기록
ord-08060253b8454e1db64e9a7901143a1d
출처 데이터셋
uspto-grants-1996_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05486513

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