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1-Pentene, 5-bromo- → Bis(3-butenyl)mercury

HRID 1030286
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HRID 1030286 반응식
[CH2:1]([Hg:6][CH2:7][CH2:8][CH2:9][CH:10]=C)[CH2:2][CH2:3][CH:4]=C.C([Mg]Br)CCC=C.BrCCCC=C.[Mg]>O1CCCC1.O>[CH2:1]([Hg:6][CH2:7][CH2:8][CH:9]=[CH2:10])[CH2:2][CH:3]=[CH2:4]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 707041-Pentene, 5-bromo-HCID 5462224MagnesiumHCID 19105421Di(pent-4-en-1-yl)mercuryHCID 178445862HCID 178445862, 화합물

생성물 1

HCID 12533408Bis(3-butenyl)mercury수율 67%

시약·촉매·용매 2

HCID 962Water용매

반응 조건

온도
60 °C

실험 절차

Preparation of bis(4-pentenyl)mercury: To a solution of 4-pentenyl magnesium bromide, prepared from 25 g of 1-bromo-4-pentene (169 mmole) and 5 g of magnesium (208 mmole) in 40 mL of tetrahydrofuran, was added dropwise at 50° C. with stirring a solution of 25.2 g of mercuric chloride (93 mmole) in 50 mL of tetrahydrofuran. After stirring for 2 hours at 60° C., the reaction mixture was hydrolyzed with water at 0°-5° C. The organic layer was separated from aqueous layer; the product was distilled to give bis-3-butenyl mercury in 67% yield. The identity of the compound was confirmed by gas chromatography and 1H NMR.

후처리

  1. additionwas added dropwise at 50° C.
  2. customThe organic layer was separated from aqueous layer
  3. distillationthe product was distilled

출처 및 근거

ORD 기록
ord-600abf639513445cbafc104f778c6e93
출처 데이터셋
uspto-grants-1992_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05104952

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이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
HCID 8028
Tetrahydrofuran
용매
2회