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2,2-Dimethoxypropane → 8-Bromo-2-(2,2-dimethyl-1,3-dioxolan-4-yl)quinoline

HRID 339670
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인쇄 미리보기

반응식

HRID 339670 반응식
[Br:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[N:10]=[C:9]([CH:12]([OH:15])[CH2:13][OH:14])[CH:8]=[CH:7]2.CO[C:18](OC)([CH3:20])[CH3:19].O.[O-2].[O-2].[O-2].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O.[Al+3].[Al+3]>CC(C)=O>[Br:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[N:10]=[C:9]([CH:12]1[CH2:13][O:14][C:18]([CH3:20])([CH3:19])[O:15]1)[CH:8]=[CH:7]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 64952,2-DimethoxypropaneHCID 672345141-(8-Bromoquinolin-2-yl)ethane-1,2-diolHCID 71586775Bentonite

생성물 1

HCID 672343698-Bromo-2-(2,2-dimethyl-1,3-dioxolan-4-yl)quinoline

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

To 1-(8-bromoquinolin-2-yl)ethane-1,2-diol (505 mg, 1.88 mmol) in acetone (5 mL) and 2,2-dimethoxypropane (5 mL, 1.88 mmol) was added Montmorillonite K 10 (1 g). The reaction mixture was stirred for 2 hours, then filtered and concentrated to give crude product.

후처리

  1. filtrationfiltered
  2. concentrationconcentrated
  3. customto give crude product

출처 및 근거

ORD 기록
ord-8ae0cdbdbda24f8f9fb12dcb9ae8e45b
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08895550B2

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