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Benzoyl Peroxide → 1-Bromo-4-(bromomethyl)-5-chloro-2-fluorobenzene

HRID 508412
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HRID 508412 반응식
[Br:1][C:2]1[C:7]([F:8])=[CH:6][C:5]([CH3:9])=[C:4]([Cl:10])[CH:3]=1.[Br:11]N1C(=O)CCC1=O.C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1>C(Cl)(Cl)(Cl)Cl.CCCCCCC>[Br:1][C:2]1[CH:3]=[C:4]([Cl:10])[C:5]([CH2:9][Br:11])=[CH:6][C:7]=1[F:8]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 7187Benzoyl PeroxideHCID 67184N-bromobutanimideHCID 27362284-Bromo-2-chloro-5-fluorotoluene

생성물 1

HCID 666667551-Bromo-4-(bromomethyl)-5-chloro-2-fluorobenzene

시약·촉매·용매 2

HCID 5943Carbon Tetrachloride용매HCID 8900Heptane용매
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온도
85 °C

실험 절차

A solution of 4-bromo-2-chloro-5-fluorotoluene (997 mg, 4.46 mmol), N-bromosuccinimide (837 mg, 4.70 mmol) and benzoyl peroxide (35 mg, 0.14 mmol) in carbon tetrachloride (20 mL) was heated to reflux at 85° C. for 18.5 hours under nitrogen. The reaction mixture was concentrated in vacuo to afford a cream solid residue. The residue was suspended in heptane (40 mL), filtered and the filtrate then concentrated in vacuo to afford the title compound a clear oil (1.35 g, 100%). The compound was used without further purification in the next step.

후처리

  1. concentrationThe reaction mixture was concentrated in vacuo
  2. customto afford a cream solid residue
  3. filtrationfiltered
  4. concentrationthe filtrate then concentrated in vacuo

출처 및 근거

ORD 기록
ord-0527604248cb4cef927ba5efaab48d78
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09096500B2

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