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Morpholine → 2-(Morpholine-4-carbonyl)cyclohexane-1-carboxylic acid

HRID 427392
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HRID 427392 반응식
[C@@H:1]12[C:10](=[O:11])[O:9][C:7](=[O:8])[C@@H:2]1[CH2:3][CH2:4][CH2:5][CH2:6]2.[NH:12]1[CH2:17][CH2:16][O:15][CH2:14][CH2:13]1>C(Cl)Cl>[N:12]1([C:7]([CH:2]2[CH2:3][CH2:4][CH2:5][CH2:6][CH:1]2[C:10]([OH:9])=[O:11])=[O:8])[CH2:17][CH2:16][O:15][CH2:14][CH2:13]1
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참가 물질

4

반응물 2

HCID 8083MorpholineHCID 641660Hexahydrophthalic anhydride, cis-

생성물 1

HCID 31145632-(Morpholine-4-carbonyl)cyclohexane-1-carboxylic acid수율 90%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of cis-1,2-cyclohexane dicarboxylic anhydride (1.0 g, 6.49 mmol) in CH2Cl2 (16 mL) was added morpholine (0.56 g, 6.49 mmol) at 0° C., the resulting mixture was allowed to stir at room temperature overnight (20 h). When complete the reaction mixture was washed with HCl (1.0 N, 20 mL) then with H2O (2×20 mL). The combined aqueous layers were extracted with CH2Cl2 (3×10 mL), and the combined organic layers were dried over MgSO4, the solvent was evaporated in vacuo to give the title compound (1.4 g, 90%/) as a white solid which was used later without further purification.

후처리

  1. washWhen complete the reaction mixture was washed with HCl (1.0 N, 20 mL)
  2. extractionThe combined aqueous layers were extracted with CH2Cl2 (3×10 mL)
  3. dry with materialthe combined organic layers were dried over MgSO4
  4. customthe solvent was evaporated in vacuo

출처 및 근거

ORD 기록
ord-ddbeeefd8af747ce8d0a080bcde97eae
출처 데이터셋
uspto-grants-2001_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06313117B1

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