Hydrochloric Acid → cis-2-(4-Bromobenzoyl)cyclopropanecarboxylic acid

HRID 2427322Notes

Reaction equation

HRID 2427322 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Al+3].[Cl-].[Cl-].[Cl-].[CH:12]12[CH2:17][CH:16]1[C:15](=[O:18])[O:14][C:13]2=[O:19].Cl>C(Cl)Cl>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:15]([C@H:16]2[CH2:17][C@H:12]2[C:13]([OH:19])=[O:14])=[O:18])=[CH:4][CH:3]=1

Participants

6

Reactant 4

HCID 313Hydrochloric AcidHCID 7961BromobenzeneHCID 27347213-Oxabicyclo(3.1.0)hexane-2,4-dioneHCID 6451240Aluminum(III) Chloride

Product 1

HCID 67147316cis-2-(4-Bromobenzoyl)cyclopropanecarboxylic acidYield 74.6%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To a cold (0° C.) stirred solution of bromobenzene (9.09 g, 57.89 mmol) and AlCl3 (18.36 g, 137.84 mmol) in dry DCM (150 mL) was added 3-oxabicyclo[3.1.0]hexane-2,4-dione (5.40 g, 48.24 mmol). The reaction mixture was stirred at rt for 3 days. The dark-red solution was then poured into ice-cold water (120 mL), and conc. HCl (10 mL) was added. The solution was stirred for few minutes, and the layers were separated. The aqueous layer was extracted with DCM and the combined organic phases were washed with water, brine, dried over Na2SO4 and concentrated to give cis-2-(4-bromobenzoyl)cyclopropanecarboxylic acid (9.69 g, 65%). LC-MS ret. time 2.50; m/z 270 (MH+); 1H NMR (400 MHz, CD2Cl2) δ 1.54 (m, 1H), 1.85 (m, 1H), 2.37 (m, 1H), 2.88 (m, 1H), 7.65 (m, 2H), 7.90 (m, 2H).

Workup

  1. additionwas added
  2. stirringThe solution was stirred for few minutes
  3. customthe layers were separated
  4. extractionThe aqueous layer was extracted with DCM
  5. washthe combined organic phases were washed with water, brine
  6. dry with materialdried over Na2SO4
  7. concentrationconcentrated

Sources & evidence

ORD record
ord-310abc4c0c284d47b9d77b366441aedf
Source dataset
uspto-grants-2011_06
Patent number
US07968576B2

Reaction notes

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