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Triphenylphosphine → 4-(2-Bromoethyl)-1,1'-biphenyl

HRID 2269729
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HRID 2269729 반응식
[Br:1]Br.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[C:22]1([C:31]2[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=2)[CH:27]=[CH:26][C:25]([CH2:28][CH2:29]O)=[CH:24][CH:23]=1>C(#N)C>[C:22]1([C:31]2[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=2)[CH:27]=[CH:26][C:25]([CH2:28][CH2:29][Br:1])=[CH:24][CH:23]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11776TriphenylphosphineHCID 24408BromineHCID 64245772-[1,1'-Biphenyl]-4-yl-1-ethanol

생성물 1

HCID 64245814-(2-Bromoethyl)-1,1'-biphenyl

시약·촉매·용매 1

HCID 6342Acetonitrile용매2회

실험 절차

Bromine (1.5 ml) was added dropwise to an acetonitrile (60 ml) solution of triphenylphosphine (5 g). After stirring for 5 minutes, an acetonitrile solution (30 ml) of 2-(4-biphenylyl)ethanol (5 g) was added to the reaction mixture. The reaction mixture was stirred at room temperature for one hour and concentrated. Diethyl ether was added to the residue. The supernatant was collected, then dried and concentrated. The residue was purified by silica gel column chromatography (eluent: IPE) to obtain 2-(4-bipenylyl)ethylbromide(6 g). 2-(4-Bipenylyl)ethyl bromide (6 g) was dissolved in methanol (100 ml), which was stirred at 70° C. for 48 hours together with potassium thiocyanate (4.0 g). The reaction mixture was concentrated, and the residue was extracted with ethyl acetate. The organic layer was washed with water, then dried and concentrated. The residue was recrystallized from ethyl acetate-hexane to obtain the entitled compound (4.1 g).

후처리

  1. stirringThe reaction mixture was stirred at room temperature for one hour
  2. concentrationconcentrated
  3. additionDiethyl ether was added to the residue
  4. customThe supernatant was collected
  5. customdried
  6. concentrationconcentrated
  7. customThe residue was purified by silica gel column chromatography (eluent: IPE)

출처 및 근거

ORD 기록
ord-144927d33aa04b4aac1a23944a2acebe
출처 데이터셋
uspto-grants-2001_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06329389B1

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