Iodine → HCID 87213766, compound

HRID 1363928Notes

Reaction equation

HRID 1363928 reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[C:4]([F:9])[C:3]=1[O:10][CH3:11].C([Li])CCC.[I:17]I.OS([O-])=O.[Na+]>C1COCC1.CCOCC>[Cl:1][C:2]1[CH:7]=[C:6]([F:8])[C:5]([I:17])=[C:4]([F:9])[C:3]=1[O:10][CH3:11]

Participants

7

Reactant 4

HCID 807IodineHCID 23665763Sodium BisulfiteHCID 66953855HCID 66953855, compoundHCID 178418339Butyllithium

Product 1

HCID 87213766HCID 87213766, compoundYield 92.6%

Reagents, catalysts & solvents 2

HCID 3283Diethyl EtherSolventHCID 8028TetrahydrofuranSolvent2×

Conditions

Temperature
-72.5 °C

Procedure

2-Chloro-4,6-difluoroanisole (2.0 g, 11 mmol) was dissolved in 20 mL anhydrous THF and cooled to −70 to −75° C. 2.5M n-Butyl lithium in hexanes (6.7 mL, 17 mmol) was added dropwise. After stirring for 75 minutes at −75° C., the mixture was treated dropwise with a solution of iodine (5.1 g, 20 mmol) in 10 mL THF. After stirring for 20 minutes, the reaction solution was allowed to warm to 25° C. over 40 minutes. The reaction mixture was diluted with Et2O (50 mL) and stirred with dilute NaHSO3 solution to destroy excess iodine. The separated aqueous phase was extracted with 20 mL Et2O. The combined ether phases were washed with saturated NaCl, dried, and evaporated to give 1-chloro-3,5-difluoro-4-iodo-2-methoxybenzene (3.1 g, 91% yield): mp 62-64° C.; GC-MS (m/z=304).

Workup

  1. stirringAfter stirring for 20 minutes
  2. temperatureto warm to 25° C. over 40 minutes
  3. customto destroy excess iodine
  4. extractionThe separated aqueous phase was extracted with 20 mL Et2O
  5. washThe combined ether phases were washed with saturated NaCl
  6. customdried
  7. customevaporated

Sources & evidence

ORD record
ord-a5d80bfd4dea4caeb6ba0a3cb0a473dd
Source dataset
uspto-grants-2011_02
Patent number
US07888287B2

Reaction notes

Loading…