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Triethylamine → 4-Bromo-N-(cyclopropylmethyl)benzamide

HRID 1272702
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HRID 1272702 반응식
[CH:1]1([CH2:4][NH2:5])[CH2:3][CH2:2]1.C(N(CC)CC)C.[Br:13][C:14]1[CH:22]=[CH:21][C:17]([C:18](Cl)=[O:19])=[CH:16][CH:15]=1>C1COCC1>[Br:13][C:14]1[CH:22]=[CH:21][C:17]([C:18]([NH:5][CH2:4][CH:1]2[CH2:3][CH2:2]2)=[O:19])=[CH:16][CH:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 685154-Bromobenzoyl chlorideHCID 75646Cyclopropanemethanamine

생성물 1

HCID 184578074-Bromo-N-(cyclopropylmethyl)benzamide수율 74.2%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Cyclopropylmethylamine (1.62 g, 22.8 mmol) and triethylamine (3 ml) were dissolved in THF (40 ml) and 4-bromobenzoylchloride (5 g, 22.8 mmol) added over 5 min at 0° C. The reaction was stirred at room temperature for 16 h, reduced to dryness under vacuum and the residue partitioned between DCM (75 ml) and water (75 ml). The aqueous was extracted with DCM (2×50 ml). The combined organic phases were washed with brine, dried (magnesium sulphate) and the solvent evaporated under vacuum. The residue was purified by flash column chromatography on silica eluting with cyclohexane/ethyl acetate (8:2). The solvent was evaporated from the product fractions under vacuum to give 4-bromo-N-cyclopropylmethylbenzamide (4.3 g, 74%). LCMS: retention time 3.00 min, MH+255.

후처리

  1. customthe residue partitioned between DCM (75 ml) and water (75 ml)
  2. extractionThe aqueous was extracted with DCM (2×50 ml)
  3. washThe combined organic phases were washed with brine
  4. dry with materialdried (magnesium sulphate)
  5. customthe solvent evaporated under vacuum
  6. customThe residue was purified by flash column chromatography on silica eluting with cyclohexane/ethyl acetate (8:2)
  7. customThe solvent was evaporated from the product fractions under vacuum

출처 및 근거

ORD 기록
ord-9d121f87227d4849ae4bb27667b7d37e
출처 데이터셋
uspto-grants-2007_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07208629B2

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