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3-(3-Bromo-1,4-dioxonaphthalen-2-yl)propanoic acid → (2R/S)-3-(3-bromo-1,4-naphthoquinon-2-yl)-2-methylpropionic acid

HRID 1527716
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인쇄 미리보기

반응식

HRID 1527716 반응식
[Br:1][C:2]1[C:11](=[O:12])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[C:4](=[O:13])[C:3]=1[CH2:14][CH:15]([CH3:21])[C:16]([O:18]CC)=[O:17].BrC1C(=O)C2C(=CC=CC=2)C(=O)C=1CCC(O)=O>CC(C)=O>[Br:1][C:2]1[C:11](=[O:12])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[C:4](=[O:13])[C:3]=1[CH2:14][CH:15]([CH3:21])[C:16]([OH:18])=[O:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 454872363-(3-Bromo-1,4-dioxonaphthalen-2-yl)propanoic acidHCID 70835151Ethyl (2R/S)-3-(3-bromo-1,4-naphthoquinon-2-yl)-2-methylpropionate

생성물 1

HCID 59583711(2R/S)-3-(3-bromo-1,4-naphthoquinon-2-yl)-2-methylpropionic acid

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

Compound 69b was prepared from racemic 68b (0.027 g, 0.08 mmol) as described above for 69a to give 0.016 g (0.05 mmol, 63%) of the product as a yellow solid following flash chromatography (1:4 acetone:hexanes 0 to 0.5% AcOH) and recrystallization from Et2O/hexanes.

후처리

  1. customto give

출처 및 근거

ORD 기록
ord-665a1d651c3a4d16868285ecab5507f0
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09089605B2

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