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Sodium Hydroxide → (2,2-dibromoethenyl)benzene

HRID 1789087
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HRID 1789087 반응식
[Br:1][CH2:2][CH2:3][C:4]1[C:5](Br)=[C:6](Br)[CH:7]=[CH:8][CH:9]=1.[OH-].[Na+].[Br-:14].C([N+](CC)(CC)CCCCC)C>C(Cl)Cl>[Br:1][C:2]([Br:14])=[CH:3][C:4]1[CH:5]=[CH:6][CH:7]=[CH:8][CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 14798Sodium HydroxideHCID 15919122N,N,N-Triethylpentan-1-aminium bromideHCID 197981311,2-Dibromo-3-(2-bromoethyl)benzene

생성물 1

HCID 161726(2,2-dibromoethenyl)benzene

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A solution of 147.90 g. (0.431 mole) of 2-bromoethyldibromobenzene in 250 ml. of methylene chloride was stirred for 7 ks (2 hours) at 5 Hz (300 rpm) at 313 K. (40° C.) with 150 g (2.25 mole) of 60 percent sodium hydroxide solution and 3.12 g. (0.0124 mole) of triethylpentyl ammonium bromide. The product was washed with three 500-ml portions of water, dried over calcium sulfate (Drierite), and stripped of solvent in a rotary evaporator at a bath temperature of 323 K. (50° C.). The yield of product was 106.97 g. (77.2 per cent of theory). GC analysis showed 27.1 percent of the desired ar-dibromostyrene, the remainder being largely unreacted starting material.

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후처리

  1. custom(40° C.)
  2. washThe product was washed with three 500-ml portions of water
  3. dry with materialdried over calcium sulfate (Drierite)
  4. customstripped of solvent in a rotary evaporator at a bath temperature of 323 K
  5. custom(50° C.)

출처 및 근거

ORD 기록
ord-872ec79cdd2e42ecb9a3d4b0e647897d
출처 데이터셋
uspto-grants-1987_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04686311

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