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3-Bromobenzaldehyde → 1-Bromo-3-(2-methyl-1-propenyl)benzene

HRID 466643
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HRID 466643 반응식
[I-].[CH:2]([P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)([CH3:4])[CH3:3].CC(C)([O-])C.[K+].[Br:30][C:31]1[CH:32]=[C:33]([CH:36]=[CH:37][CH:38]=1)[CH:34]=O>C1COCC1.C1OCCOCCOCCOCCOCCOC1>[Br:30][C:31]1[CH:38]=[CH:37][CH:36]=[C:33]([CH:34]=[C:2]([CH3:4])[CH3:3])[CH:32]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 765833-BromobenzaldehydeHCID 2723783Isopropyltriphenylphosphonium iodideHCID 23665647Potassium tert-butoxide

생성물 1

HCID 217068361-Bromo-3-(2-methyl-1-propenyl)benzene수율 75.3%

시약·촉매·용매 2

HCID 2855718-Crown-6촉매HCID 8028
Tetrahydrofuran
용매
2회

실험 절차

To a stirred slurry of 17.83 g (41.2 mmol) of isopropyltriphenylphosphonium iodide and 300 mg (1.1 mmol) of 18-crown-6 in 50 mL of THF under nitrogen at 5° C. was added 4.60 g (41.0 mmol) of potassium t-butoxide over 5 minutes. The resulting deep red-orange slurry was stirred 10 minutes and then a solution of 4.31 mL (37.0 mmol) of 3-bromobenzaldehyde in 40 mL of THF was added at a rate to keep the temperature below 10° C. The resulting bright yellow slurry was stirred for 20 minutes and then poured into 300 mL of hexanes. The solids were filtered off and the filtrate evaporated. This residue was purified by flash chromatography (5×15 cm column) and eluted with hexanes to provide 5.88 g (75%) of title compound as a colorless oil.

후처리

  1. customthe temperature below 10° C
  2. stirringThe resulting bright yellow slurry was stirred for 20 minutes
  3. filtrationThe solids were filtered off
  4. customthe filtrate evaporated
  5. customThis residue was purified by flash chromatography (5×15 cm column)
  6. washeluted with hexanes

출처 및 근거

ORD 기록
ord-2e4bd4a7bf1b4401a81feba32fb102f2
출처 데이터셋
uspto-grants-1992_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05157027

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