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ethyl (2S*,3R*)-2-amino-3-hydroxy-4-methyl-pentanoate → Npc168081

HRID 530564
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인쇄 미리보기

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HRID 530564 반응식
[NH2:1][C@@H:2]([C@H:8]([OH:12])[CH:9]([CH3:11])[CH3:10])[C:3]([O:5]CC)=[O:4]>Cl>[NH2:1][C@@H:2]([C@H:8]([OH:12])[CH:9]([CH3:11])[CH3:10])[C:3]([OH:5])=[O:4]
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참가 물질

3

반응물 1

HCID 86700007ethyl (2S*,3R*)-2-amino-3-hydroxy-4-methyl-pentanoate

생성물 1

HCID 6994743Npc168081수율 117.5%

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

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온도
130 °C

실험 절차

In a 35 ml microwave vial, ethyl (2S*,3R*)-2-amino-3-hydroxy-4-methyl-pentanoate (0.232 g, 1.33 mmol) was dissolved in a 6.0 M HCl aqueous solution (25 mL) and stirred at 130° C. for 1 h. The reaction mixture was extracted with Et2O (3×15 mL), the aqueous phase was concentrated under reduced pressure resulting in a white solid (0.23 g, 81%), which was used without further purification in the following step. MS (ESI) m/z: 148 [M−H]+; (ESI) m/z: 146 [M−H]−. 1H NMR (DMSO-d6) δ 0.87 (d, J=6.64 Hz, 3H), 0.93 (d, J=6.50 Hz, 3H), 1.74 (tq, J=5.79, 6.46, 11.64 Hz, 1H), 3.51-3.60 (m, 1H), 3.92 (s, 1H), 5.76 (s, 1H), 8.12 (s, 3H), 13.72 (s, 1H) [see also Tetrahedron 2001, 57, 8267-8276].

후처리

  1. extractionThe reaction mixture was extracted with Et2O (3×15 mL)
  2. concentrationthe aqueous phase was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-4d3627a1c9574c34b2c32326a17828de
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09353075B2

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