반응 #2028877

ord-fc2de7eae42f49f0a11bfcac06f22eb2

반응 방정식

CC(=O)Cl
acetyl chloride
[Al+3].[Cl-].[Cl-].[Cl-]
Aluminum chloride
COc1ccccc1F
2-fluoroanisole
COc1ccc(C(C)=O)cc1F
3′-fluoro-4′-methoxyacetophenone

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타fitted with a mechanical stirrer
  2. 2
    온도cooled by means of an ice bath
  3. 3
    온도maintaining the temperature between 5°-10° C
  4. 4
    기타The resultant layers were separated
  5. 5
    추출the aqueous layer was extracted with methylene chloride (2×250 mL)
  6. 6
    세척The combined organic layers were washed with water (2×150 mL)
  7. 7
    건조dried over magnesium sulfate
  8. 8
    농축concentrated to 300 mL
  9. 9
    기타Hexanes crystallized from the mixture

실험 절차

Aluminum chloride (80.0 g, 0.6 mol) and chloroform (750 mL) were placed in a 2 L three-necked round bottom flask fitted with a mechanical stirrer and cooled by means of an ice bath. To the stirred solution was added acetyl chloride (51.0 g, 0.65 mol) dropwise, maintaining the temperature between 5°-10° C. The mixture was allowed to stir for 10 minutes at 5° C. before the dropwise addition at 5°-10° C. of 2-fluoroanisole (63.06 g, 0.5 mol. The mixture was stirred at 0°-10° C. for 1 hour and poured into ice (1 L). The resultant layers were separated and the aqueous layer was extracted with methylene chloride (2×250 mL). The combined organic layers were washed with water (2×150 mL), dried over magnesium sulfate, and concentrated to 300 mL. Hexanes crystallized from the mixture: mp 92°-94° C.; 1H NMR (d6-DMSO) 7.8 (m, 2H), 7.3 (t, J=8.7Hz, 1H), 3.9 (s, 3H), 2.5 (s, 3H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: USRE044048E1uspto-grants-2013_03