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Pyridine → 3,5-Di-t-butyl-4-hydroxy-benzylpyridinium chloride

HRID 1729755
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인쇄 미리보기

반응식

HRID 1729755 반응식
[C:1]([C:5]1[CH:6]=[C:7]([CH:10]=[C:11]([C:14]([CH3:17])([CH3:16])[CH3:15])[C:12]=1[OH:13])[CH2:8][Cl:9])([CH3:4])([CH3:3])[CH3:2].[N:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>CC(C)=O>[Cl-:9].[C:1]([C:5]1[CH:6]=[C:7]([CH:10]=[C:11]([C:14]([CH3:17])([CH3:16])[CH3:15])[C:12]=1[OH:13])[CH2:8][N+:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)([CH3:4])([CH3:3])[CH3:2]
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참가 물질

4

반응물 2

HCID 1049PyridineHCID 123786012,6-Di-tert-butyl-4-(chloromethyl)phenol

생성물 1

HCID 104969033,5-Di-t-butyl-4-hydroxy-benzylpyridinium chloride

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

1271/2 Grams of 3,5-di-tert.butyl-4-hydroxybenzyl chloride was added dropwise, in 40 minutes, to a solution of 44.0 grams of pyridine in 500 milliliters of acetone. The mixture was stirred briefly and was then filtered, yielding 159 grams of 3,5-di-tert.butyl-4-hydroxybenzyl-pyridinium chloride, with a melting point of 239°-240° C. (with decomposition). This represents 95 percent of theory.

후처리

  1. filtrationwas then filtered

출처 및 근거

ORD 기록
ord-c5cc984e108a46e3a77c7c75e1063d16
출처 데이터셋
uspto-grants-1976_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03989738

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