Sodium hydride → Ammonium Hydroxide

HRID 1840064Notes

Reaction equation

HRID 1840064 reaction equation
[O:1]([C:8]1[CH:9]=[C:10]([CH:12]=[CH:13][CH:14]=1)[NH2:11])C1C=CC=CC=1.[H-].[Na+].FC(F)(F)O[C:20]1[CH:21]=[C:22]([CH:25]=[CH:26][CH:27]=1)[CH2:23]Br>C1CCCCC1>[OH-:1].[NH4+:11].[CH2:23]([NH:11][C:10]1[CH:9]=[CH:8][CH:14]=[CH:13][CH:12]=1)[C:22]1[CH:25]=[CH:26][CH:27]=[CH:20][CH:21]=1

Participants

6

Reactant 3

HCID 24758Sodium hydrideHCID 771353-PhenoxyanilineHCID 7371761-(Bromomethyl)-3-(trifluoromethoxy)benzene2×

Product 2

HCID 14923Ammonium HydroxideHCID 66028Benzylaniline

Reagents, catalysts & solvents 1

HCID 8078CyclohexaneSolvent

Procedure

To a solution of 3-phenoxyaniline (10.9 g, 58.8 mmol) in 100 mL of cyclohexane was added solid NaH (60% in mineral oil, 1.96 g, 49 mmol). Then 3-trifluoromethoxybenzyl bromide (10.0 g, 39.2 mmol) was added dropwise under a nitrogen atmosphere, and the mixture was heated to reflux for 18 h, at which time TLC analysis indicated that no 3-trifluoromethoxybenzyl bromide remained. The reaction miure was cooled to room temperature and quenched with water, then extracted with ether. The ether layer was washed with water and brine, then dried over MgSO4, and evaporated to give crude product. The crude product was purified by flash column chromatography on silica gd eluting with 1:7:0.01 of ethyl acetate:hexane:ammonium hydroxide to give the desired N-benzylaniline product, which contained a small portion of dibenzylated amine. This product was further purified by conversion to the corresponding HCl salt to give 11.0 g (73%) of the desired N-(3-phenoxyphenyl)-N-[(3-trifluoromethoxy)phenyl]methyl]amine hydrochloride product. HRMS calcd. for C20H16NO2F3: 360.1211 [M+H]+, found 360.1208.

Workup

  1. temperaturethe mixture was heated
  2. temperatureto reflux for 18 h, at which time TLC analysis
  3. customquenched with water
  4. extractionextracted with ether
  5. washThe ether layer was washed with water and brine
  6. dry with materialdried over MgSO4
  7. customevaporated
  8. customto give crude product
  9. customThe crude product was purified by flash column chromatography on silica
  10. washgd eluting with 1:7:0.01 of ethyl acetate

Sources & evidence

ORD record
ord-0805a976daed4e0a91d9b6dd93b4f265
Source dataset
uspto-grants-2004_01
Patent number
US06677375B2

Reaction notes

Loading…