Sodium Hydroxide → 1-[(2-Furanylcarbonyl)amino]cyclohexanecarboxylic acid

HRID 1392409노트

반응식

HRID 1392409 반응식
[O:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]([NH:8][C:9]1([C:15]([O:17]C)=[O:16])[CH2:14][CH2:13][CH2:12][CH2:11][CH2:10]1)=[O:7].[OH-].[Na+]>CO>[O:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]([NH:8][C:9]1([C:15]([OH:17])=[O:16])[CH2:14][CH2:13][CH2:12][CH2:11][CH2:10]1)=[O:7]

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 17464840methyl 1-[N-(furan-2-ylcarbonyl)amino]-1-cyclohexanecarboxylate

생성물 1

HCID 174552541-[(2-Furanylcarbonyl)amino]cyclohexanecarboxylic acid수율 67.3%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To the solution of methyl 1-[N-(furan-2-ylcarbonyl)amino]-1-cyclohexanecarboxylate (9.6 g) obtained in Step 1 in 100 ml of methanol, was added 2N-sodium hydroxide solution (50 ml). The reaction mixture was refluxed for 3 hours and concentrated. The resulting residue was diluted with 150 ml of water and washed with 100 ml of diethyl ether. 6N-hydrochloride was added dropwise to the resulting aqueous layer to adjust the pH of the solution to pH 3. The resulting white solid was filtered and dried to give the titled compound (6.1 g).

후처리

  1. temperatureThe reaction mixture was refluxed for 3 hours
  2. concentrationconcentrated
  3. additionThe resulting residue was diluted with 150 ml of water
  4. washwashed with 100 ml of diethyl ether
  5. addition6N-hydrochloride was added dropwise to the resulting aqueous layer
  6. filtrationThe resulting white solid was filtered
  7. customdried

출처 및 근거

ORD 기록
ord-799b78f15edb4ce1ac8f00e026c29467
출처 데이터셋
uspto-grants-2008_03
특허 번호
US07342027B2

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