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Ethyl 4-(dibenzylamino)-2-methylcyclopentanecarboxylate → 4-(Dibenzylamino)-2-methylcyclopentanecarboxylic acid

HRID 1969749
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HRID 1969749 반응식
[CH2:1]([N:8]([CH2:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)[CH:9]1[CH2:13][CH:12]([C:14]([O:16]CC)=[O:15])[CH:11]([CH3:19])[CH2:10]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>Cl.O1CCOCC1>[CH2:20]([N:8]([CH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)[CH:9]1[CH2:13][CH:12]([C:14]([OH:16])=[O:15])[CH:11]([CH3:19])[CH2:10]1)[C:21]1[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=1
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참가 물질

4

반응물 1

HCID 58010318Ethyl 4-(dibenzylamino)-2-methylcyclopentanecarboxylate

생성물 1

HCID 585575354-(Dibenzylamino)-2-methylcyclopentanecarboxylic acid수율 98.3%

시약·촉매·용매 2

HCID 313Hydrochloric Acid용매HCID 312751,4-Dioxane용매

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온도
60 °C

실험 절차

Ethyl 4-(dibenzylamino)-2-methylcyclopentanecarboxylate (3.65 g, 10.38 mmol) was dissolved in a mixture of HCl (6 N aqueous, 20 mL) and 1,4-dioxane (50 mL) and the resulting mixture was heated at about 60° C. for about 72 h. The organic solvent was removed under reduced pressure. The aqueous phase was neutralized by the addition of saturated aqueous NaHCO3 (40 mL) and extracted with EtOAc (50 mL). The organic phase was washed with brine (40 mL), dried over anhydrous MgSO4 and concd under reduced pressure to yield 4-(dibenzylamino)-2-methylcyclopentanecarboxylic acid (3.3 g, 98%) as a white amorphous solid: LC/MS (Table 1, Method a) Rt=1.66 min; MS m/z 324 (M+H)+.

후처리

  1. customThe organic solvent was removed under reduced pressure
  2. additionThe aqueous phase was neutralized by the addition of saturated aqueous NaHCO3 (40 mL)
  3. extractionextracted with EtOAc (50 mL)
  4. washThe organic phase was washed with brine (40 mL)
  5. dry with materialdried over anhydrous MgSO4 and concd under reduced pressure

출처 및 근거

ORD 기록
ord-afa26b44ac9740c7b73aac6c03b6b679
출처 데이터셋
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08426411B2

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