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Triphenylbismuth → Diphenylbismuthanyl Bromide

HRID 2261506
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HRID 2261506 반응식
[C:1]1([Bi:7](C2C=CC=CC=2)[C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Br:20][Bi](Br)Br>C1COCC1>[C:1]1([Bi:7]([Br:20])[C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 11774TriphenylbismuthHCID 82232bismuth(III) bromide

생성물 1

HCID 13026286Diphenylbismuthanyl Bromide수율 83%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
0 °C

실험 절차

In 400 ml of THF was dissolved 22.014 g (50 mmol) of triphenylbismuthine (Tokyo Kasei Co., Ltd.) under nitrogen atmosphere. The solution was cooled to 0° C. and thereto was slowly added dropwise 11.231 g (25 mmol) of tribromobismuthine (Aldrich Corp.) (30 minutes). The mixture was stirred to room temperature for 1 hour. The yellow precipitate was filtered and dried in a vacuum. The obtained precipitate was recrystallized from benzene, giving 27.422 g (62 mmol: yield 83%) of yellow powdery product.

후처리

  1. filtrationThe yellow precipitate was filtered
  2. customdried in a vacuum
  3. customThe obtained precipitate was recrystallized from benzene
  4. customgiving 27.422 g (62 mmol: yield 83%) of yellow powdery product

출처 및 근거

ORD 기록
ord-6de6a5d0fb9b4c64a493fe578b70f983
출처 데이터셋
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07847043B2

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