Potassium Iodide → 3-(2-Phenyl-4-thiazolylmethoxy)benzenacetonitrile

HRID 1029852Notes

Reaction equation

HRID 1029852 reaction equation
[OH:1][C:2]1[CH:3]=[C:4]([CH2:8][C:9]#[N:10])[CH:5]=[CH:6][CH:7]=1.Cl.Cl[CH2:13][C:14]1[N:15]=[C:16]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[S:17][CH:18]=1.C(=O)([O-])[O-].[Cs+].[Cs+].[I-].[K+]>CC(C)=O>[C:19]1([C:16]2[S:17][CH:18]=[C:14]([CH2:13][O:1][C:2]3[CH:3]=[C:4]([CH2:8][C:9]#[N:10])[CH:5]=[CH:6][CH:7]=3)[N:15]=2)[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=1

Participants

6

Procedure

To a solution of 14.0 g (0.105 mol) of 3-hydroxyphenylacetonitrile in 500 ml of acetone were added 25.9 g (0.105 mol) of 4-chloromethyl-2-phenylthiazole hydrochloride and 34.2 g (0.105 mol) of cesium carbonate and 1 g of potassium iodide and the slurry is heated to reflux for 20 hours. The mixture is filtered and the solution is concentrated in vacuo to obtain crystals. Recrystallization from ethyl acetate gives 14.0 g (43%) crystals, m.p. 108°-110° C. The product is used without further purification in subsequent reactions.

Workup

  1. temperaturethe slurry is heated
  2. temperatureto reflux for 20 hours
  3. filtrationThe mixture is filtered
  4. concentrationthe solution is concentrated in vacuo
  5. customto obtain crystals
  6. customRecrystallization from ethyl acetate

Sources & evidence

ORD record
ord-f7d9d64233ec4a839600c2a053c1f185
Source dataset
uspto-grants-1992_04
Patent number
US05103014

Reaction notes

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