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Methylamine → 4-bromo-N,2-dimethylbenzamide

HRID 2090473
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HRID 2090473 반응식
[Br:1][C:2]1[CH:10]=[CH:9][C:5]([C:6](O)=[O:7])=[C:4]([CH3:11])[CH:3]=1.C(Cl)(=O)C(Cl)=O.CN.[CH2:20]([N:22](CC)CC)C>C(Cl)Cl.CN(C)C=O>[Br:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([NH:22][CH3:20])=[O:7])=[C:4]([CH3:11])[CH:3]=1
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참가 물질

7

반응물 4

HCID 6329MethylamineHCID 8471TriethylamineHCID 65578Oxalyl chlorideHCID 995704-Bromo-2-methylbenzoic acid

생성물 1

HCID 575165344-bromo-N,2-dimethylbenzamide수율 93.4%

시약·촉매·용매 2

HCID 6228Dimethylformamide용매
HCID 6344
Dichloromethane
용매

실험 절차

N,N-Dimethylformamide (10 uL) was added to a mixture of 4-bromo-2-methylbenzoic acid (1.0 g, 0.0046 mol) in oxalyl chloride (2.0 mL, 0.023 mol). The mixture was stirred at r.t. overnight. The volatiles were removed under reduced pressure. The residue was dissolved in methylene chloride (2 mL). To the solution was added to a mixture of methylamine (0.41 mL, 0.0093 mol) and triethylamine (1.3 mL, 0.0093 mol) in DCM (10 ml). After 30 min, the reaction mixture was quenched with aqueous sodium carbonate (10 mL) and extracted with DCM (3×20 mL). The organic layers were washed with brine, dried over Na2SO4, filtered. The solvents were removed under reduced pressure to give a crude product (980 mg, 92.4%). LCMS (M+H)+: m/z=228.1/230.2.

후처리

  1. customThe volatiles were removed under reduced pressure
  2. dissolutionThe residue was dissolved in methylene chloride (2 mL)
  3. waitAfter 30 min
  4. customthe reaction mixture was quenched with aqueous sodium carbonate (10 mL)
  5. extractionextracted with DCM (3×20 mL)
  6. washThe organic layers were washed with brine
  7. dry with materialdried over Na2SO4
  8. filtrationfiltered
  9. customThe solvents were removed under reduced pressure

출처 및 근거

ORD 기록
ord-6dbd51bc16824583a77b77e87394c7d1
출처 데이터셋
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08436008B2

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