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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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p-Toluenesulfonic acid → 6-Bromo-2,2,4,4-tetramethylchroman

HRID 51664
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인쇄 미리보기

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HRID 51664 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5](O)=[C:4]([C:9]([CH3:16])([CH3:15])[CH2:10][C:11]([OH:14])([CH3:13])[CH3:12])[CH:3]=1.C1(C)C=CC(S(O)(=O)=O)=CC=1>C1C=CC=CC=1>[Br:1][C:2]1[CH:3]=[C:4]2[C:5](=[CH:6][CH:7]=1)[O:14][C:11]([CH3:13])([CH3:12])[CH2:10][C:9]2([CH3:16])[CH3:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6101p-Toluenesulfonic acidHCID 225688104-Bromo-2-(3-hydroxy-1,1,3-trimethyl-butyl)-phenol

생성물 1

HCID 121370056-Bromo-2,2,4,4-tetramethylchroman수율 80%

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

A solution of 4-bromo-2-(3-hydroxy-1,1,3-trimethyl-butyl)-phenol (1.1 g, 3.92 mmol) and p-toluene sulfonic acid (0.744 g, 3.92 mmol) in benzene (20 mL) was refluxed overnight. The reaction mixture cooled to ambient temperature, filtered on silica gel and washed with 10% ethyl acetate in hexane. The filtrate and washings were evaporated in vacuo to an oil which was subjected to flash column chromatography over silica gel (230-400 mesh) using 5% ethyl acetate in hexane as the eluent to afford the title compound as a pale yellow oil (0.84 g, 80%).

후처리

  1. filtrationfiltered on silica gel
  2. washwashed with 10% ethyl acetate in hexane
  3. customThe filtrate and washings were evaporated in vacuo to an oil which

출처 및 근거

ORD 기록
ord-c3702489ca08444e9c93bfc77972e233
출처 데이터셋
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06713647B2

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