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1,7-Dibromoheptane → 1-Bromo-7-phenylheptane

HRID 1030179
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HRID 1030179 반응식
Br[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][Br:9].[C:10]1([Li])[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1>C1COCC1>[Br:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1
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참가 물질

4

반응물 2

HCID 783091,7-DibromoheptaneHCID 178506676HCID 178506676, 화합물

생성물 1

HCID 27356031-Bromo-7-phenylheptane수율 49%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a stirred solution of 1,7-dibromoheptane (49 g, 0.18 mol) (Aldrich) in THF (300 ml), at -30° C. to -40° C., under N2, was added, dropwise, during 3 h, a solution of phenyllithium (15 g, 0.18 mol) in cyclohexane-ether (2.0M solution, Aldrich). The reaction was allowed to stir at -10° C. to -20° C. for 3 h and at room temperature overnight. After slow, careful dilution with H2O (50 ml), the aqueous layer was extracted with Et2O (2×150 ml). The extracts and the organic layer were combined, dried (Na2SO4) and concentrated to a yellow oil. Distillation through a Vigreaux column provided 22.5 g of 1-bromo-7-phenylheptane, bp 84°-88° C. (0.2 mm), nD24 1.5220.

후처리

  1. extractionAfter slow, careful dilution with H2O (50 ml), the aqueous layer was extracted with Et2O (2×150 ml)
  2. dry with materialdried (Na2SO4)
  3. concentrationconcentrated to a yellow oil
  4. distillationDistillation through a Vigreaux column

출처 및 근거

ORD 기록
ord-2c758457bf634fa5a98080cde8f68dfc
출처 데이터셋
uspto-grants-1992_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05104885

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