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Acetic Acid → tert-Butyl 2-(tetrahydrofuran-3-yl)hydrazinecarboxylate

HRID 1043877
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HRID 1043877 반응식
[O:1]1[CH2:5][CH2:4][C:3](=[N:6][NH:7][C:8]([O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:9])[CH2:2]1.C(O)(=O)C.C([BH3-])#N.[Na+].[OH-].[Na+]>O>[O:1]1[CH2:5][CH2:4][CH:3]([NH:6][NH:7][C:8]([O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:9])[CH2:2]1
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참가 물질

6

반응물 4

HCID 176Acetic AcidHCID 14798Sodium HydroxideHCID 5003444Sodium cyanoborohydrideHCID 72309493tert-butyl 2-(dihydrofuran-3(2H)-ylidene)hydrazinecarboxylate

생성물 1

HCID 54775639tert-Butyl 2-(tetrahydrofuran-3-yl)hydrazinecarboxylate수율 87.8%

시약·촉매·용매 1

HCID 962
Water
용매

실험 절차

t-butyl 2-[dihydrofuran-3(2H)-ylidene]hydrazinecarboxylate (17.26 g) was suspended in water (130 mL). Acetic acid (57.2 mL) was added to the suspension at room temperature. The mixture was stirred at room temperature for one hour. Sodium cyanoborohydride (5.36 g) was added to the solution in small portions. The mixed solution was stirred at room temperature for two hours. The reaction mixture was cooled to 0° C. The reaction mixture was neutralized by adding a 5 N aqueous sodium hydroxide solution. The mixture was extracted with chloroform. The organic layer was dried over anhydrous magnesium sulfate and then filtered. The filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (5% methanol/ethyl acetate). The title compound (15.3 g) was obtained.

후처리

  1. stirringThe mixed solution was stirred at room temperature for two hours
  2. temperatureThe reaction mixture was cooled to 0° C
  3. extractionThe mixture was extracted with chloroform
  4. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  5. filtrationfiltered
  6. concentrationThe filtrate was concentrated under reduced pressure
  7. customThe residue was purified by silica gel column chromatography (5% methanol/ethyl acetate)

출처 및 근거

ORD 기록
ord-fbe183f54fa246dd90f649787478c154
출처 데이터셋
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08563565B2

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