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Ammonium Chloride → HCID 69559116, 화합물

HRID 2213024
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HRID 2213024 반응식
[N:1]1([C:12]([O:14][C:15]([CH3:18])([CH3:17])[CH3:16])=[O:13])[CH2:6][CH2:5][CH:4]([C:7]([O:9][CH2:10][CH3:11])=[O:8])[CH2:3][CH2:2]1.C[Si](C)(C)[N-][Si](C)(C)C.[K+].Br[CH2:30][C:31]([CH3:33])=[CH2:32].[Cl-].[NH4+]>O1CCCC1.O>[CH3:32][C:31](=[CH2:30])[CH2:33][C:4]1([C:7]([O:9][CH2:10][CH3:11])=[O:8])[CH2:3][CH2:2][N:1]([C:12]([O:14][C:15]([CH3:17])([CH3:16])[CH3:18])=[O:13])[CH2:6][CH2:5]1
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참가 물질

7

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HCID 25517Ammonium ChlorideHCID 3577853-Bromo-2-methyl-1-propeneHCID 27588121-Tert-butyl 4-ethyl piperidine-1,4-dicarboxylateHCID 3251421Potassium bis(trimethylsilyl)amide

생성물 1

HCID 69559116HCID 69559116, 화합물수율 99.4%

시약·촉매·용매 2

HCID 962
Water
용매
HCID 8028Tetrahydrofuran용매2회

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온도
-78 °C

실험 절차

A solution of 1-(1,1-dimethylethyl) 4-ethyl 1,4-piperidinedicarboxylate (12.85 g, 50 mmol) in tetrahydrofuran (50 mL) was added slowly to a stirred, cooled (−78° C.) solution of potassium hexamethyldisilazide (14.96 g, 75 mmol) in tetrahydrofuran (75 mL), maintaining the internal temperature below −65° C. The mixture was stirred at −78° C. for 30 minutes, then 3-bromo-2-methylpropene (7.56 mL, 10.12 g, 75 mmol) was added dropwise over 5 minutes. The mixture was stirred at −78° C. for 1 hour, then saturated aqueous ammonium chloride (200 mL) was added and the mixture was warmed to room temperature. Water (100 mL) was added and the mixture was extracted with ethyl acetate (3×200 mL). The combined organic fractions were washed with aqueous citric acid (10%, 3×200 mL), saturated aqueous sodium hydrogen carbonate (200 mL) and brine (200 mL), dried (MgSO4) and the solvent was evaporated under reduced pressure to give the title compound as a pale yellow oil (15.48 g, 99%). m/z (ES+) 256 (M+1-C4H8).

후처리

  1. temperaturemaintaining the internal temperature below −65° C
  2. stirringThe mixture was stirred at −78° C. for 1 hour
  3. temperaturethe mixture was warmed to room temperature
  4. extractionthe mixture was extracted with ethyl acetate (3×200 mL)
  5. washThe combined organic fractions were washed with aqueous citric acid (10%, 3×200 mL), saturated aqueous sodium hydrogen carbonate (200 mL) and brine (200 mL)
  6. dry with materialdried (MgSO4)
  7. customthe solvent was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-565af6031dae45718f9e802271fd124d
출처 데이터셋
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07105507B2

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