Ethanol → HCID 20378394, compound
Reaction equation
[F:1][C:2]1[CH:21]=[CH:20][C:5]([O:6][CH:7]([CH3:19])[CH2:8][NH:9][C:10]2[CH:18]=[CH:17][CH:16]=[CH:15][C:11]=2C([O-])=O)=[CH:4][CH:3]=1.[OH-:22].[K+].[CH2:24]([OH:26])C>O.Cl.C(Cl)(Cl)Cl.CCCCCC>[F:1][C:2]1[CH:3]=[CH:4][C:5]([O:6][CH:7]([CH3:19])[CH2:8][NH:9][C:10]2[CH:11]=[CH:15][C:16]([C:24]([OH:26])=[O:22])=[CH:17][CH:18]=2)=[CH:20][CH:21]=1Participants
8
Procedure
A solution of 2.6 g of ethyl p-[2-(4-fluorophenoxy)propylaminobenzoate in 100 ml of 95% ethanol containing 2.7 g of potassium hydroxide was heated to reflux for 2 hours. The reaction was cooled, diluted with 100 ml of water and neutralized with 37% hydrochloric acid. The solid was collected and dried giving a white solid which was dissolved in 25 ml of chloroform and diluted with 1 ml of hexane giving a solid with a m.p. 171°-172° C.
Workup
- temperatureto reflux for 2 hours
- temperatureThe reaction was cooled
- customThe solid was collected
- customdried
- customgiving a white solid which
Sources & evidence
- ORD record
- ord-7dfb2948814a4c8285f2bfc886bd03d3
- Source dataset
- uspto-grants-1980_01
- Patent number
- US04182776
Reaction notes
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