Hydrochloric Acid → HCID 70921801, compound

HRID 2365921Notes

Reaction equation

HRID 2365921 reaction equation
Cl.[CH2:2]([O:9][C:10]1[CH:15]=[C:14]([O:16][CH2:17][C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[C:13](N)=[CH:12][C:11]=1[F:25])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.N([O-])=O.[Na+].[I-:30].[K+].[Cl-].[NH4+]>CN(C)C=O.O.[Cu](I)I>[CH2:2]([O:9][C:10]1[CH:15]=[C:14]([O:16][CH2:17][C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[C:13]([I:30])=[CH:12][C:11]=1[F:25])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1

Participants

9

Conditions

Temperature
0 °C

Procedure

7 ml of 6M hydrochloric acid are added to a solution of 3.20 g (9.9 mmol, 1 eq) of 1,5-bis(benzyloxy)-2-fluoro-4-aminobenzene in 40 ml of N,N-dimethylformamide, cooled to 0° C. 683 mg (9.9 mmol, 1 eq) of sodium nitrite in solution in 7 ml of water are added and the reaction medium is stirred at 0° C. for 1 hour. 1.64 g (9.9 mmol, 1 eq) of potassium iodide in solution in 8 ml of water are added, followed by 190 mg (1.0 mmol, 0.1 eq) of copper iodide, and then the reaction medium is stirred at ambient temperature overnight. The reaction medium is treated with a saturated solution of ammonium chloride and extracted with ethyl acetate. The organic phases are combined, washed with a saturated solution of sodium chloride, dried over magnesium sulphate, filtered and evaporated. The residue is chromatographed on silica gel, elution being carried out with 75/25 heptane/dichloromethane. 3.59 g of 1,5-bis(benzyloxy)-2-fluoro-4-iodobenzene are obtained.

Workup

  1. stirringthe reaction medium is stirred at ambient temperature overnight
  2. extractionextracted with ethyl acetate
  3. washwashed with a saturated solution of sodium chloride
  4. dry with materialdried over magnesium sulphate
  5. filtrationfiltered
  6. customevaporated
  7. customThe residue is chromatographed on silica gel, elution

Sources & evidence

ORD record
ord-5b57cdafd1a14e81b213fb5adcff7d10
Source dataset
uspto-grants-2014_04
Patent number
US08697726B2

Reaction notes

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