Benzyl Bromide → (S)-benzyl 2-(dibenzylamino)pentanoate

HRID 1972323노트

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HRID 1972323 반응식
[OH-:1].[Na+].[C:3](=[O:6])([O-])[O-].[K+].[K+].[NH2:9][C@@H:10]([CH2:14][CH2:15][CH3:16])[C:11](O)=O.[CH2:17](Br)[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>O>[CH2:17]([N:9]([CH2:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)[C@@H:10]([CH2:14][CH2:15][CH3:16])[C:11]([O:6][CH2:3][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)=[O:1])[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1

참가 물질

6

반응물 4

HCID 7498Benzyl BromideHCID 11430Potassium CarbonateHCID 14798Sodium HydroxideHCID 65098L-Norvaline

생성물 1

HCID 44223288(S)-benzyl 2-(dibenzylamino)pentanoate수율 132.9%

시약·촉매·용매 1

HCID 962Water용매

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온도
0 °C

실험 절차

Sodium hydroxide (0.513 Kg; 12.82 moles) and potassium carbonate (1.77 Kg, 12.82 moles) were dissolved in water (7.5 L) and cooled to 0° C. The resulting solution was treated with (S)-2-aminopentanoic acid (L-norvaline, 0.75 Kg; 6.41 moles) slowly at between 0-5° C. The stirred suspension was heated at 90° C. and benzyl bromide (4.385 Kg, 25.64 moles) was added dropwise. Heating was continued for a further 12 hours at 90° C. The reaction mixture was then cooled to ambient temperature, and extracted with ethyl acetate (2×6 liters). The layers were separated and the aqueous phase extracted twice with ethyl acetate. The combined organic extracts were dried over sodium sulfate, and the solvent removed under reduced pressure to obtain 3.3 Kg of crude (S)-benzyl 2-(dibenzylamino)pentanoate, a compound of formula (3), as a brown oil. This material was used in the next reaction without further purification.

후처리

  1. temperatureThe stirred suspension was heated at 90° C.
  2. temperatureHeating
  3. temperatureThe reaction mixture was then cooled to ambient temperature
  4. extractionextracted with ethyl acetate (2×6 liters)
  5. customThe layers were separated
  6. extractionthe aqueous phase extracted twice with ethyl acetate
  7. dry with materialThe combined organic extracts were dried over sodium sulfate
  8. customthe solvent removed under reduced pressure

출처 및 근거

ORD 기록
ord-f7b38c2c6f8f4157bf7f2030d294d5a7
출처 데이터셋
uspto-grants-2013_04
특허 번호
US08431733B2

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