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Hydrochloric Acid → Methyl 4-bromo-2-chlorobenzeneacetate

HRID 906840
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HRID 906840 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]#N)=[C:4]([Cl:11])[CH:3]=1.[CH3:12][OH:13].Cl.[OH2:15]>>[CH3:12][O:13][C:9](=[O:15])[CH2:8][C:5]1[CH:6]=[CH:7][C:2]([Br:1])=[CH:3][C:4]=1[Cl:11]
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참가 물질

5

반응물 4

HCID 313Hydrochloric AcidHCID 887MethanolHCID 962WaterHCID 58762522(4-Bromo-2-chlorophenyl)acetonitrile

생성물 1

HCID 57624630Methyl 4-bromo-2-chlorobenzeneacetate수율 80%

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온도
0 °C

실험 절차

(4-Bromo-2-chloro-phenyl)-acetonitrile (1.98 g, 8.6 mmoles) was dissolved into MeOH (50 mL) and water (5 mL), and the resulting homogeneous mixture was chilled to 0° C. To this stirring (cold) mixture was slowly (carefully) added concentrated HCl (25 mL). After the addition was complete the mixture was refluxed for 16 hours. After this period the reaction mixture was combined with ice and the resulting heterogeneous mixture was extracted with diethyl ether (3×50 mL). The combined ethereal layer was washed with brine, dried over anhydrous MgSO4, and evaporated in vacuo to yield clean (4-bromo-2-chloro-phenyl)-acetic acid methyl ester (2.3 g, 80%). 1H-NMR (CDCl3): δ 7.56 (d, J=2.0 Hz, 1H), 7.37 (dd, J′=8.3 Hz, J″=2.0 Hz, 1H), 7.16 (d, J=8.3 Hz, 1H), 3.73 (s, 2H), 3.72 (s, 3H).

후처리

  1. additionAfter the addition
  2. temperaturewas refluxed for 16 hours
  3. waitAfter this period the reaction mixture was combined with ice
  4. extractionthe resulting heterogeneous mixture was extracted with diethyl ether (3×50 mL)
  5. washThe combined ethereal layer was washed with brine
  6. dry with materialdried over anhydrous MgSO4
  7. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-3b3bc9eb3b5e403fb82369dfbe611056
출처 데이터셋
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08013001B2

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