Benzene → HCID 21411013, compound

HRID 1415174Notes

Reaction equation

HRID 1415174 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8](Cl)[C:9]2[CH:14]=[CH:13][C:12]([F:15])=[CH:11][CH:10]=2)=[CH:4][CH:3]=1.[OH:17][CH2:18][CH2:19][NH:20][C:21](=[O:23])[CH3:22].C(=O)([O-])[O-].[K+].[K+].C1C=CC=CC=1>O>[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([C:9]2[CH:14]=[CH:13][C:12]([F:15])=[CH:11][CH:10]=2)[O:17][CH2:18][CH2:19][NH:20][C:21](=[O:23])[CH3:22])=[CH:4][CH:3]=1

Participants

6

Procedure

A mixture of 25.4 g (0.1 mole) of bis(p-fluorophenyl)methyl chloride, 10.3 g (0.1 mole) of N-(2-hydroxyethyl)acetamide (prepared according to F. J. McQuillin et. al., J. Chem. Soc. 1955, 2966), 14 g of potassium carbonate and 100 ml of benzene is refluxed for 5 hours. After cooling, the reaction mixture is poured into water. The aqueous layer is extracted with dichloromethane and the combined organic layers are dried over potassium carbonate and concentrated by evaporation of solvent. The residue is crystallised from toluene. N-{2-[B is(p-fluorophenyl)methoxy]ethyl}-acetamide, m.p. 112°-113.5° C., is obtained.

Workup

  1. temperatureis refluxed for 5 hours
  2. temperatureAfter cooling
  3. extractionThe aqueous layer is extracted with dichloromethane
  4. dry with materialthe combined organic layers are dried over potassium carbonate
  5. concentrationconcentrated by evaporation of solvent
  6. customThe residue is crystallised from toluene

Sources & evidence

ORD record
ord-6413a54137ed429d8ef3395e5fcaafd5
Source dataset
uspto-grants-1977_01
Patent number
US04003932

Reaction notes

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