tert-Butanol → tert-Butyl 10-(3-chloro-2,6-dihydroxy-5-formyl-4-methylphenyl)decanoate

HRID 59632노트

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HRID 59632 반응식
C(OC(C(F)(F)F)=O)(C(F)(F)F)=O.[Cl:14][C:15]1[C:16]([OH:37])=[C:17]([CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][C:34]([OH:36])=[O:35])[C:18]([OH:24])=[C:19]([CH:22]=[O:23])[C:20]=1[CH3:21].[CH3:38][C:39](O)([CH3:41])[CH3:40].C([O-])(O)=O.[Na+]>C1(C)C=CC=CC=1>[Cl:14][C:15]1[C:16]([OH:37])=[C:17]([CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][C:34]([O:36][C:39]([CH3:41])([CH3:40])[CH3:38])=[O:35])[C:18]([OH:24])=[C:19]([CH:22]=[O:23])[C:20]=1[CH3:21]

참가 물질

6

실험 절차

TFAA (0.20 ml, 1.4 mmol) was added to a suspension of Compound 215-11-COOH (144 mg, 0.403 mmol) in toluene (5 ml) at 0° C., and the mixture was allowed to warm to room temperature with stirring for 30 minutes. After checking for complete dissolution of the raw material, the mixture was again cooled to 0° C. tBuOH (0.40 ml, 4.2 mmol) was added to the cooled mixture, which was allowed to warm to room temperature with stirring for 15 hours. A saturated aqueous NaHCO3 solution was added to the reaction solution, which was extracted with EtOAc twice after stirring for 5 minutes. The combined organic layer was washed with a saturated aqueous NaCl solution, and was dried over anhydrous Na2SO4. After evaporation of the solvent, the residue was purified by column chromatography on silica gel (Hexane:EtOAc=7:1 to 4:1) followed by PTLC (Hexane:EtOAc=7:1) to yield the target product (28 mg, 17%).

후처리

  1. additionwas added to the cooled mixture, which
  2. temperatureto warm to room temperature
  3. stirringwith stirring for 15 hours
  4. extractionwas extracted with EtOAc twice
  5. stirringafter stirring for 5 minutes
  6. washThe combined organic layer was washed with a saturated aqueous NaCl solution
  7. dry with materialwas dried over anhydrous Na2SO4
  8. customAfter evaporation of the solvent
  9. customthe residue was purified by column chromatography on silica gel (Hexane:EtOAc=7:1 to 4:1)

출처 및 근거

ORD 기록
ord-c417d92c592d4fa59c0ee801cef0a675
출처 데이터셋
uspto-grants-2016_09
특허 번호
US09440913B2

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