Acetic Acid → 4-(2,2-Dichlorocyclopropyl)phenol

HRID 1605122Notes

Reaction equation

HRID 1605122 reaction equation
[Cl:1][C:2]1([Cl:12])[CH2:4][CH:3]1[C:5]1[CH:11]=[CH:10][C:8](N)=[CH:7][CH:6]=1.C(O)(=[O:15])C.N([O-])=O.[Na+].S(=O)(=O)(O)O>O>[Cl:1][C:2]1([Cl:12])[CH2:4][CH:3]1[C:5]1[CH:11]=[CH:10][C:8]([OH:15])=[CH:7][CH:6]=1

Participants

6

Procedure

A solution of 50 g. (0.248 mole) of p-(2,2-dichlorocyclopropyl)aniline in 185 ml. of glacial acetic acid was cooled to about 10°C., and a solution of 18.9 g. (0.273 mole) of sodium nitrite in 185 ml. of water was added dropwise to the stirred solution. A thick slurry formed and this was added portionwise to a stirred solution of 160 ml. of concentrated sulfuric acid in 320 ml. of water held at 100°-105°C. The reaction mixture was stirred at 100 ± 5°C. for 10 minutes, then cooled and diluted with water. The resulting product was collected by filtration, dissolved in ether and washed with sodium bicarbonate solution. The ether solution was then extracted with sodium hydroxide solution, and the sodium hydroxide solution was acidified and extracted with ether. The ether solution was dried and concentrated in vacuo, and the residue (18 g.) was steam distilled affording 9 g. of a yellow gum which crystallized when triturated with ether. There was thus obtained 8 g. of p-(2,2-dichlorocyclopropyl)phenol, m.p. 54.5°-56°C.

Workup

  1. customA thick slurry formed
  2. additionthis was added portionwise to a stirred solution of 160 ml
  3. customheld at 100°-105°C
  4. temperaturecooled
  5. filtrationThe resulting product was collected by filtration
  6. dissolutiondissolved in ether
  7. washwashed with sodium bicarbonate solution
  8. extractionThe ether solution was then extracted with sodium hydroxide solution
  9. extractionextracted with ether
  10. dry with materialThe ether solution was dried
  11. concentrationconcentrated in vacuo
  12. distillationdistilled
  13. customaffording 9 g
  14. customof a yellow gum which crystallized when
  15. customtriturated with ether

Sources & evidence

ORD record
ord-fe7f46951e0843b7a3013cc150a0a47a
Source dataset
uspto-grants-1976_04
Patent number
US03948973

Reaction notes

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