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Ethanol → ethyl (2R)-2-amino-6-acetamidohexanoate

HRID 1397879
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HRID 1397879 반응식
[NH:1](C(OC(C)(C)C)=O)[C@H:2]([C:11]([OH:13])=[O:12])[CH2:3][CH2:4][CH2:5][CH2:6][NH:7][C:8]([CH3:10])=[O:9].O=S(Cl)Cl.[CH3:25][CH2:26]O>>[C:8]([NH:7][CH2:6][CH2:5][CH2:4][CH2:3][C@@H:2]([NH2:1])[C:11]([O:13][CH2:25][CH3:26])=[O:12])(=[O:9])[CH3:10]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 702EthanolHCID 24386Thionyl ChlorideHCID 7016049Boc-Lys(Ac)-OH

생성물 1

HCID 86723916ethyl (2R)-2-amino-6-acetamidohexanoate수율 80%

반응 조건

온도
-10 °C

실험 절차

Boc-Lys(Ac)-OH (1 equivalent, 0.2 g, 0.69 mmol) was dissolved in EtOH (2 mL). The reaction mixture was cooled at −10° C., and SOCl2 (1.5 equivalent, 76 μl, 1.035 mmol) was added dropwise. The mixture was allowed to warm to room temperature, then heated at 40° C. for 20 h (TLC control). The reaction mixture was concentrated and the crude was purified by flash chromatography (CH2Cl2/MeOH) to afford the compound (120 mg, 80%) as a white solid Rf=0.62 (CH2Cl2/MeOH 70/30).

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

후처리

  1. temperatureto warm to room temperature
  2. temperatureheated at 40° C. for 20 h (TLC control)
  3. concentrationThe reaction mixture was concentrated
  4. customthe crude was purified by flash chromatography (CH2Cl2/MeOH)

출처 및 근거

ORD 기록
ord-74d0a55492bf4d2680e2dd777ec9c3c2
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08901295B2

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