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Diethyl Ether → Methyl 4-{[(tert-butoxy)carbonyl]amino}bicyclo[2.2.1]heptane-1-carboxylate

HRID 1854334
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HRID 1854334 반응식
[CH3:1][O:2][C:3]([C:5]12[CH2:11][C:8](C(O)=O)([CH2:9][CH2:10]1)[CH2:7][CH2:6]2)=[O:4].C1(P([N:29]=[N+]=[N-])(C2C=CC=CC=2)=O)C=CC=CC=1.[C:32]([OH:36])([CH3:35])([CH3:34])[CH3:33].CC[O:39][CH2:40]C>C1(C)C=CC=CC=1>[C:32]([O:36][C:40]([NH:29][C:8]12[CH2:11][C:5]([C:3]([O:2][CH3:1])=[O:4])([CH2:6][CH2:7]1)[CH2:10][CH2:9]2)=[O:39])([CH3:35])([CH3:34])[CH3:33]
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참가 물질

6

반응물 4

HCID 3283Diethyl EtherHCID 6386tert-ButanolHCID 199401P,P-Diphenylphosphinic azideHCID 137617744-(Methoxycarbonyl)bicyclo(2.2.1)heptane-1-carboxylic acid

생성물 1

HCID 58009867Methyl 4-{[(tert-butoxy)carbonyl]amino}bicyclo[2.2.1]heptane-1-carboxylate수율 81%

시약·촉매·용매 1

HCID 1140
Toluene
용매

실험 절차

To a solution of 4-(methoxycarbonyl)bicyclo[2.2.1]heptane-1-carboxylic acid (2.01 g, 10.1 mmol) in toluene (30 mL) was added diphenyl phosphoryl azide (2.20 mL, 10.2 mmol) and TEA (1.60 mL, 11.5 mmol). The mixture was stirred at room temperature for about 1 h followed by heating at about 50° C. for about 3 h and further heating at about 70° C. for about 2 h. The reaction was cooled to room temperature and concentrated to dryness under reduced pressure. The residue was diluted in tert-butanol (10.0 mL, 105 mmol) and the mixture was heated at about 80° C. for about 16 h. The reaction mixture was cooled to room temperature and dissolved in Et2O (50 mL). The organic layer was washed with water, aqueous 1 M NaOH, water, and brine (25 mL each). The organic layer was dried over anhydrous Na2SO4, filtered, and concentrated to provide methyl 4-(tert-butoxycarbonylamino)bicyclo[2.2.1]heptane-1-carboxylate as an off-white solid (2.22 g, 81%): 1H NMR (400 MHz, DMSO-d6) δ 7.03 (s, 1H), 3.59 (s, 3H), 1.95-1.74 (m, 6H), 1.60 (s, 4H), 1.37 (s, 9H).

후처리

  1. temperatureby heating at about 50° C. for about 3 h
  2. temperaturefurther heating at about 70° C. for about 2 h
  3. temperatureThe reaction was cooled to room temperature
  4. concentrationconcentrated to dryness under reduced pressure
  5. temperaturethe mixture was heated at about 80° C. for about 16 h
  6. temperatureThe reaction mixture was cooled to room temperature
  7. washThe organic layer was washed with water, aqueous 1 M NaOH, water, and brine (25 mL each)
  8. dry with materialThe organic layer was dried over anhydrous Na2SO4
  9. filtrationfiltered
  10. concentrationconcentrated

출처 및 근거

ORD 기록
ord-fc46c9561e2546b990cb21e9104a3cf7
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08962629B2

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