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Hydrochloric Acid → Methyl 2-bromo-5-chloro-4-methylbenzoate

HRID 1037061
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HRID 1037061 반응식
N[C:2]1[C:3]([CH3:13])=[CH:4][C:5]([Br:12])=[C:6]([CH:11]=1)[C:7]([O:9][CH3:10])=[O:8].N([O-])=O.[Na+].[ClH:18]>O.[Cu]Cl>[Br:12][C:5]1[CH:4]=[C:3]([CH3:13])[C:2]([Cl:18])=[CH:11][C:6]=1[C:7]([O:9][CH3:10])=[O:8]
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참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 23668193Sodium NitriteHCID 56924477Methyl 5-amino-2-bromo-4-methylbenzoate

생성물 1

HCID 53330616Methyl 2-bromo-5-chloro-4-methylbenzoate수율 64.4%

시약·촉매·용매 2

HCID 62652Cuprous chloride촉매HCID 962Water용매

실험 절차

To a solution of methyl 5-amino-2-bromo-4-methylbenzoate (4.86 g, 20 mmol) in hydrochloric acid (6N, 50 mL) was added sodium nitrite (1.38 g, 20 mmol) carefully at −5° C. After one hour, the obtained mixture was added to a boiling solution of copper(I) chloride (3.96 g, 40 mmol) in water (50 mL) dropwise and the resulting mixture was refluxed with stirring for 2 h. The mixture was cooled to rt and extracted with ethyl acetate (2×50 mL). The combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated. The residue was purified by silica gel column chromatography eluted with PE to give methyl 2-bromo-5-chloro-4-methylbenzoate (3.4 g, yield 64.4%). 1H NMR (400 MHz, DMSO-d6): δ 7.82 (s, 1H), 7.81 (s, 1H), 3.85 (s, 3H), 2.51 (s, 3H) ppm; MS: m/z=265.0 (M+1, ESI+).

후처리

  1. temperaturethe resulting mixture was refluxed
  2. extractionextracted with ethyl acetate (2×50 mL)
  3. washThe combined organic layers were washed with brine
  4. dry with materialdried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe residue was purified by silica gel column chromatography
  8. washeluted with PE

출처 및 근거

ORD 기록
ord-f816c1553ed84b38ae0bd0b335aaddc9
출처 데이터셋
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08546357B2

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