Potassium Carbonate → HCID 22006769, compound

HRID 377706Notes

Reaction equation

HRID 377706 reaction equation
[CH2:1]([C:3]1[CH:4]=[C:5]([OH:27])[CH:6]=[C:7]([CH3:26])[C:8]=1[O:9][CH2:10][CH2:11][CH2:12][NH:13][C:14](=[O:25])[C:15]1[CH:20]=[CH:19][C:18]([C:21]([F:24])([F:23])[F:22])=[CH:17][CH:16]=1)[CH3:2].C(=O)([O-])[O-].[K+].[K+].[Cl:34][C:35]([Cl:39])=[CH:36][CH2:37]Cl>CN(C)C=O>[CH2:1]([C:3]1[CH:4]=[C:5]([O:27][CH2:37][CH:36]=[C:35]([Cl:39])[Cl:34])[CH:6]=[C:7]([CH3:26])[C:8]=1[O:9][CH2:10][CH2:11][CH2:12][NH:13][C:14](=[O:25])[C:15]1[CH:20]=[CH:19][C:18]([C:21]([F:24])([F:22])[F:23])=[CH:17][CH:16]=1)[CH3:2]

Participants

5

Procedure

To a mixture of 0.66 g of 3-ethyl-5-methyl-4-(3-(4-(trifluoromethyl)benzamido)propyloxy)phenol, 0.29 g of potassium carbonate and 20 ml of N,N-dimethylformamide was added dropwise a mixed solution of 0.28 g of 1,1,3-trichloropropene and 5 ml of N,N-dimethylformamide, while stirring at room temperature. After stirring at room temperature for 6 hours, the reaction mixture was poured into ice water and extracted twice with 50 ml of diethyl ether. The ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and then concentrated to give crude crystals. The crude crystals were ground and washed with n-hexane, which afforded 0.48 g of 3-ethyl-5-methyl-1-(3,3-dichloro-2-propenyloxy)-4-(3-(4-(trifluoromethyl)benzamido)propyloxy)benzene (58% yield), m.p., 92.2° C.

Workup

  1. stirringAfter stirring at room temperature for 6 hours
  2. extractionextracted twice with 50 ml of diethyl ether
  3. washwashed with water
  4. dry with materialdried over anhydrous magnesium sulfate
  5. concentrationconcentrated
  6. customto give crude crystals
  7. washwashed with n-hexane, which

Sources & evidence

ORD record
ord-58d4947b0f694f91b6504e1a604db68b
Source dataset
uspto-grants-2000_02
Patent number
US06028100

Reaction notes

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