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Hydroxide → HCID 89500331, 화합물

HRID 575540
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HRID 575540 반응식
[Br-].[CH2:2]([N+:15]1([CH3:21])[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16]1)[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][N+:8]1([CH3:14])[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9]1.[Br-].[OH-:23]>>[OH-:23].[CH2:2]([N+:15]1([CH3:21])[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16]1)[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][N+:8]1([CH3:14])[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13]1.[OH-:23]
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참가 물질

3

반응물 2

HCID 961HydroxideHCID 713306561,1'-(Hexane-1,6-diyl)bis(1-methylpiperidin-1-ium) dibromide

생성물 1

HCID 89500331HCID 89500331, 화합물

실험 절차

1,1′-(hexane-1,6-diyl)bis(1-methylpiperidin-1-ium) bromide was subsequently converted to a hydroxide solution by column ion-exchange using an excess of MTO-DOWEX SBR LCNG(OH) resin. Distilled water was eluted through the column until the pH was less than 11 and the resulting solution concentrated to the desired concentration, typically ˜20 wt %. The concentration was confirmed by acid-base titration and by 1H NMR.

후처리

  1. washDistilled water was eluted through the column until the pH was less than 11
  2. concentrationthe resulting solution concentrated to the desired
  3. concentrationconcentration, typically ˜20 wt %
  4. concentrationThe concentration

출처 및 근거

ORD 기록
ord-0431d568823b4c4690142333dae53622
출처 데이터셋
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09035058B2

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