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tert-Butyl hydroperoxide → N-Benzyloxycarbonyl-4-[(R*)-2-methyl-sulfinylphenyl]piperidine

HRID 1738983
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HRID 1738983 반응식
C(OC(N1CC[CH:14]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=2[S@@:23](C)=[O:24])CC1)=O)C1C=CC=CC=1.C([C@](C([O-])=O)(O)[C@](CC)(O)C([O-])=O)C.[CH2:40]([O:47][C:48]([N:50]1[CH2:55][CH2:54][CH:53](C2C=CC=CC=2SC)[CH2:52][CH2:51]1)=[O:49])[C:41]1[CH:46]=[CH:45][CH:44]=[CH:43][CH:42]=1.C(OO)(C)(C)C>ClCCl.CC(C)[O-].CC(C)[O-].CC(C)[O-].CC(C)[O-].[Ti+4].O>[CH2:40]([O:47][C:48]([N:50]1[CH2:55][CH2:54][CH:53]([C:22]2[C@@H:17]([CH3:14])[C:18](=[S:23]=[O:24])[CH:19]=[CH:20][CH:21]=2)[CH2:52][CH2:51]1)=[O:49])[C:41]1[CH:46]=[CH:45][CH:44]=[CH:43][CH:42]=1
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8

반응물 4

HCID 6410tert-Butyl hydroperoxideHCID 111106201-Benzyloxycarbonyl-4(2-methylthiophenyl)piperidineHCID 29414049diethyl-D-tartarateHCID 53634760N-Benzyloxycarbonyl-4-[(R*)-2-methylsulfinylphenyl]-piperidine

생성물 1

HCID 86750107N-Benzyloxycarbonyl-4-[(R*)-2-methyl-sulfinylphenyl]piperidine

시약·촉매·용매 3

HCID 11026
Titanium isopropoxide
촉매
HCID 962Water용매2회
HCID 6344Dichloromethane용매

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온도
-15 °C

실험 절차

N-Benzyloxycarbonyl-4-[(R*)-2-methylsulfinylphenyl]-piperidine. To a solution of diethyl-D-tartarate (3.4 mL) in dichloromethane (50 mL) was added titanium tetraisopropoxide (3.0 mL) followed by water (0.18 mL). The resulting solution was stirred vigorously for 30 minutes, treated with N-benzyloxycarbony-4-(2-methylthiophenyl)piperidine (3.41 g), and cooled to -15° C. The reaction mixture was treated with tert-butylhydroperoxide (2 mL) drop wise over a period of 1 minute, and stirred at -15° C. for 40 hours. Water (4 mL) was added, and the solution was stirred vigorously for 1 hour and filtered through a bed of diatomous earth. The filtrate was stirred with 5% aqueous sodium hydroxide (100 mL) for 1 hour and was washed with brine (50 mL). The aqueous layer was extracted with dichloromethane and the combined organic layers were washed (brine), dried (anhydrous sodium sulfate), and evaporated to give a solid product which was crystallized from diisopropyl ether to afford N-Benzyloxycarbonyl-4-[(R*)-2-methyl-sulfinylphenyl]piperidine (3.0 g).

후처리

  1. stirringstirred at -15° C. for 40 hours
  2. stirringthe solution was stirred vigorously for 1 hour
  3. filtrationfiltered through a bed of diatomous earth
  4. stirringThe filtrate was stirred with 5% aqueous sodium hydroxide (100 mL) for 1 hour
  5. washwas washed with brine (50 mL)
  6. extractionThe aqueous layer was extracted with dichloromethane
  7. washthe combined organic layers were washed (brine)
  8. dry with materialdried (anhydrous sodium sulfate)
  9. customevaporated
  10. customto give a solid product which
  11. customwas crystallized from diisopropyl ether

출처 및 근거

ORD 기록
ord-6d5d11753e7b4ce993376a10ae3961a3
출처 데이터셋
uspto-grants-1999_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05965576

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