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methyl (2S)-2-{[(tert-butoxy)carbonyl]amino}-4-phenylbutanoate → Boc-homophenylalaninal

HRID 2072667
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인쇄 미리보기

반응식

HRID 2072667 반응식
C[O:2][C:3](=O)[C@H:4]([CH2:13][CH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[NH:5][C:6]([O:8][C:9]([CH3:12])([CH3:11])[CH3:10])=[O:7]>C1(C)C=CC=CC=1>[C:6]([NH:5][C@H:4]([CH:3]=[O:2])[CH2:13][CH2:14][C:15]1[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=1)([O:8][C:9]([CH3:10])([CH3:12])[CH3:11])=[O:7]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 11220096methyl (2S)-2-{[(tert-butoxy)carbonyl]amino}-4-phenylbutanoate

생성물 1

HCID 10264740Boc-homophenylalaninal

시약·촉매·용매 1

HCID 1140Toluene용매2회

반응 조건

온도
-80 °C

실험 절차

2.93 g of N-BOC homo phenylalanine methyl ester (10 mmol) are dissolved in 25 ml of absolute toluene under nitrogen and the solution is cooled to -80° C. 20 ml of -20% strength DIBA in toluene are added dropwise and the temperature maintained. Since the reaction was not complete after 1.5 h a further 3 ml of 20% strength DIBA were added.

후처리

  1. temperaturethe temperature maintained
이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
  • additiona further 3 ml of 20% strength DIBA were added
  • 출처 및 근거

    ORD 기록
    ord-152a117c7af2493ba3bd35e0ffadc29a
    출처 데이터셋
    uspto-grants-1990_04
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04914087

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