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Acetic Acid → 8-Isopropyl-2,2,4,4-tetramethyl-chroman-6-carboxylic acid 4-(2-carboxy-vinyl)-phenyl ester

HRID 2377353
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HRID 2377353 반응식
C([SiH](C)C)(C)(C)C.C(N(CC)CC)C.C([O:22][C:23]([CH:25]=[CH:26][C:27]1[CH:32]=[CH:31][C:30]([O:33][C:34]([C:36]2[CH:37]=[C:38]3[C:43](=[C:44]([CH:46]([CH3:48])[CH3:47])[CH:45]=2)[O:42][C:41]([CH3:50])([CH3:49])[CH2:40][C:39]3([CH3:52])[CH3:51])=[O:35])=[CH:29][CH:28]=1)=[O:24])C1C=CC=CC=1.C(O)(=O)C>ClCCl.O.O1CCCC1.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[C:23]([CH:25]=[CH:26][C:27]1[CH:28]=[CH:29][C:30]([O:33][C:34]([C:36]2[CH:37]=[C:38]3[C:43](=[C:44]([CH:46]([CH3:47])[CH3:48])[CH:45]=2)[O:42][C:41]([CH3:50])([CH3:49])[CH2:40][C:39]3([CH3:51])[CH3:52])=[O:35])=[CH:31][CH:32]=1)([OH:24])=[O:22]
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참가 물질

9

반응물 4

HCID 176Acetic AcidHCID 8471TriethylamineHCID 5072427tert-ButyldimethylsilaneHCID 690737328-Isopropyl-2,2,4,4-tetramethyl-chroman-6-carboxylic acid 4-(2-benzyloxycarbonyl-vinyl)-phenyl ester2회

생성물 1

HCID 690714768-Isopropyl-2,2,4,4-tetramethyl-chroman-6-carboxylic acid 4-(2-carboxy-vinyl)-phenyl ester수율 13.5%

시약·촉매·용매 4

HCID 167845palladium(II) acetate촉매HCID 962Water용매2회HCID 6344Dichloromethane용매2회HCID 8028Tetrahydrofuran용매

실험 절차

A suspension of t-butyldimethyl silane (0.3 mL, 1.85 mmol), palladium(II)acetate (0.013 g, 0.06 mmol) and triethyl amine (0.03 mL, 0.2 mmol) in anhydrous dichloromethane (2 mL) under argon was treated with a solution of 8-isopropyl-2,2,4,4-tetramethyl-chroman-6-carboxylic acid 4-(2-benzyloxycarbonyl-vinyl)-phenyl ester (Intermediate 35, 0.063 g, 0.123 mmol) in dichloromethane (2 mL) and the resulting reaction mixture was stirred overnight at ambient temperature. The reaction mixture was quenched with water and extracted with diethyl ether. The organic extract was dried over anhydrous sodium sulfate, filtered and evaporated to a residue that was subjected to flash column chromatography to yield an intermediate that was treated with acetic acid (1 mL) in water (0.3 mL) and tetrahydrofuran (0.3 mL) at ambient temperature for 1 h. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic extract was dried over anhydrous sodium sulfate, filtered and evaporated to a residue that was subjected to preparative reverse phase HPLC using 10% water in acetonitrile as the mobile phase to afford the title compound (0.007 g).

후처리

  1. customthe resulting reaction mixture
  2. customThe reaction mixture was quenched with water
  3. extractionextracted with diethyl ether
  4. extractionThe organic extract
  5. dry with materialwas dried over anhydrous sodium sulfate
  6. filtrationfiltered
  7. customevaporated to a residue that
  8. customto yield an intermediate
  9. extractionextracted with ethyl acetate
  10. extractionThe organic extract
  11. dry with materialwas dried over anhydrous sodium sulfate
  12. filtrationfiltered
  13. customevaporated to a residue that

출처 및 근거

ORD 기록
ord-fe25deb49a1b40e4984b28a548a01103
출처 데이터셋
uspto-grants-2008_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07468391B2

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