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Hydrochloric Acid → HCID 178501085, 화합물

HRID 2260568
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HRID 2260568 반응식
CC(C)([O-])C.[K+].[C:7]([NH:10][C:11]([CH:14]1[CH2:19][CH2:18][CH:17]([C:20]([O:22][CH3:23])=[O:21])[CH2:16][CH2:15]1)([CH3:13])[CH3:12])(=[O:9])[CH3:8].Cl>CO>[C:7]([NH:10][C:11]([C@H:14]1[CH2:15][CH2:16][C@H:17]([C:20]([O:22][CH3:23])=[O:21])[CH2:18][CH2:19]1)([CH3:13])[CH3:12])(=[O:9])[CH3:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 18998535Methyl 4-(1-acetamido-1-methylethyl)cyclohexanecarboxylateHCID 23665647Potassium tert-butoxide

생성물 1

HCID 178501085HCID 178501085, 화합물수율 79.5%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

Potassium tert-butoxide (30.0 g) was added to a solution (150 ml) of a cis- and trans- mixture of methyl 4-(1-acetamido-1-methylethyl)cyclohexanecarboxylate (30.8 g) in methanol and the mixture was refluxed under heating for 40 hours. After completion of the reaction, the residue obtained by concentration under reduced pressure was poured into ice water, neutralized with conc. hydrochloric acid and extracted with chloroform. The extract was washed with water, dried and concentrated under reduced pressure. The resultant crystals were recrystallized from methanol to give 24.5 g of methyl trans-4-(1-acetamido-1-methylethyl)cyclohexanecarboxylate.

후처리

  1. temperaturethe mixture was refluxed
  2. temperatureunder heating for 40 hours
  3. customAfter completion of the reaction
  4. customthe residue obtained by concentration under reduced pressure
  5. extractionextracted with chloroform
  6. washThe extract was washed with water
  7. customdried
  8. concentrationconcentrated under reduced pressure
  9. customThe resultant crystals were recrystallized from methanol

출처 및 근거

ORD 기록
ord-ce740386962342fb85f58eba5d86a087
출처 데이터셋
uspto-grants-1995_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05478838

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