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N-bromobutanimide → Dimethyl 3-(bromomethyl)phthalate

HRID 240669
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HRID 240669 반응식
[CH3:1][O:2][C:3](=[O:15])[C:4]1[C:5](=[C:10]([CH3:14])[CH:11]=[CH:12][CH:13]=1)[C:6]([O:8][CH3:9])=[O:7].[Br:16]N1C(=O)CCC1=O>C(#N)C>[CH3:1][O:2][C:3](=[O:15])[C:4]1[C:5](=[C:10]([CH2:14][Br:16])[CH:11]=[CH:12][CH:13]=1)[C:6]([O:8][CH3:9])=[O:7]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 67184N-bromobutanimideHCID 12562468Dimethyl 3-methylphthalate

생성물 1

HCID 22464988Dimethyl 3-(bromomethyl)phthalate수율 83.6%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

반응 조건

온도
70 °C

실험 절차

A stirred mixture of 3-methyl-phthalic dimethyl ester (12.1 g, 57.9 mmol) and N-bromosuccinimide (12.4 g, 69.5 mmol) in acetonitrile (150 mL) was heated at 70° C. (oil bath), while a 200 W light bulb situated 2 cm away was shining on the reaction mixture overnight. The resulting mixture was cooled and concentrated. The residue was dissolved in ethyl acetate (150 mL), washed with water (3×50 mL) and brine (50 mL), and dried (MgSO4). Solvent was removed in vacuo, and the residue was purified by flash chromatography (SiO2, Hexane:EtOAc 8:2) to give 3-bromomethyl-phthalic dimethyl ester (13.9 g, 83%) as a solid: 1H NMR (CDCl3) δ 7.94-7.90 (dd, J=1.1 and 7.9 Hz, 1H), 7.65-7.62 (dd, J=1.0 and 6.9 Hz, 1H), 7.47 (t, J=7.8H, 1H), 4.54 (s, 2H), 3.97 (s, 3H), 3.90 (s, 3H).

후처리

  1. customaway was shining on the reaction mixture overnight
  2. temperatureThe resulting mixture was cooled
  3. concentrationconcentrated
  4. dissolutionThe residue was dissolved in ethyl acetate (150 mL)
  5. washwashed with water (3×50 mL) and brine (50 mL)
  6. dry with materialdried (MgSO4)
  7. customSolvent was removed in vacuo
  8. customthe residue was purified by flash chromatography (SiO2, Hexane:EtOAc 8:2)

출처 및 근거

ORD 기록
ord-62a5be5a8edc4526aa871ecb08e24a1d
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08648096B2

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