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Boron trifluoride etherate → 2-Ethoxyethyl 2-fluoro-4-(hexadecylamino)benzoate

HRID 1389092
Notes
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Reaction equation

HRID 1389092 reaction equation
[F:1][C:2]1[CH:10]=[C:9]([NH:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH3:27])[CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[CH2:28]([O:30][CH2:31][CH2:32]O)[CH3:29].B(F)(F)F.CCOCC>C1(C)C=CC=CC=1>[F:1][C:2]1[CH:10]=[C:9]([NH:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH3:27])[CH:8]=[CH:7][C:3]=1[C:4]([O:6][CH2:29][CH2:28][O:30][CH2:31][CH3:32])=[O:5]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 8000Boron trifluoride etherate2×HCID 8076Glycol monoethyl etherHCID 205364112-Fluoro-4-(hexadecylamino)benzoic acid

Product 1

HCID 205364602-Ethoxyethyl 2-fluoro-4-(hexadecylamino)benzoate

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent

Procedure

A solution of 11.8 g of 2-fluoro-4-(hexadecylamino)-benzoic acid, 1.00 g. of 2-ethoxyethanol and 5.35 ml of boron trifluoride etherate in 200 ml of toluene is stirred under reflux for 48 hours. The solution is treated with an additional 5.35 ml of boron trifluoride etherate and refluxing is continued for 120 hours. Dilution with water and methylene chloride followed by filtration affords 2-ethoxyethyl 2-fluoro-4-(hexadecylamino)benzoate as a white solid.

Workup

  1. temperatureunder reflux for 48 hours
  2. temperaturerefluxing
  3. filtrationDilution with water and methylene chloride followed by filtration

Sources & evidence

ORD record
ord-d25f1093e52f48de917f6a88b97746f6
Source dataset
uspto-grants-1981_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04243609

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes