18-Crown-6 → HCID 13827113, compound

HRID 978475Notes

Reaction equation

HRID 978475 reaction equation
[S-:1][C:2]#[N:3].[K+].C1OCCOCCOCCOCCOCCOC1.[F:23][C:24]1[CH:32]=[CH:31][CH:30]=[C:29]([F:33])[C:25]=1[C:26](Cl)=[O:27].[Cl:34][C:35]1[C:44]2[C:39](=[CH:40][CH:41]=[CH:42][CH:43]=2)[C:38]([O:45][C:46]2[C:52]([Cl:53])=[CH:51][C:49]([NH2:50])=[CH:48][C:47]=2[Cl:54])=[CH:37][CH:36]=1>CC#N.O>[Cl:34][C:35]1[C:44]2[C:39](=[CH:40][CH:41]=[CH:42][CH:43]=2)[C:38]([O:45][C:46]2[C:47]([Cl:54])=[CH:48][C:49]([NH:50][C:2]([NH:3][C:26](=[O:27])[C:25]3[C:24]([F:23])=[CH:32][CH:31]=[CH:30][C:29]=3[F:33])=[S:1])=[CH:51][C:52]=2[Cl:53])=[CH:37][CH:36]=1

Participants

7

Reactant 4

HCID 2855718-Crown-6HCID 874382,6-Difluorobenzoyl chlorideHCID 516872Potassium thiocyanateHCID 138271123,5-Dichloro-4-[(4-chloronaphthalen-1-yl)oxy]aniline

Product 1

HCID 13827113HCID 13827113, compound

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 6342AcetonitrileSolvent2×

Conditions

Temperature
0 °C

Procedure

To a mixture of 1.4 g of potassium thiocyanate and 1.0 mg of 18-Crown-6 in 15 ml CH3CN which was cooled to 0° C. and placed under an atmosphere of nitrogen was slowly added a solution of 23 g of 2,6-diflurobenzoyl chloride in 15 ml of CH3CN. The reaction mixture was stirred for 0.5 hr at 0° C. and then allowed to warm to room temperature. After 0.5 hr at an IR spectrum of an aliquot indicated complete disappearance of the acid chloride. To the reaction mixture was then added 4.0 g of 4-(4-chloro-1-naphthoxy)-3,5-dichloroaniline as a powder. After 0.5 hr at ambient temperature the reaction mixture was poured into 125 ml of cold water. A buff colored solid precipitated and was filtered. The filter cake was then washed with 120 ml of a 5:1 H2O:CH3CN solution. The crystals were then dried overnight in a vacuum oven at 50° C. This afforded 5.6 g of the desired thiourea as a pale yellow crystalline powder. mp 193°-195° C. NMR (D6 -DMSO): 6.43 (d, J-10 Hz, 1H), 7.0-817 (m, 10H contains singlet at 8.13), 12.35 (s, 1H), 12.62 (s, 1H).

Workup

  1. temperatureto warm to room temperature
  2. waitAfter 0.5 hr at an IR spectrum of an aliquot indicated complete
  3. customprecipitated
  4. filtrationwas filtered
  5. washThe filter cake was then washed with 120 ml of a 5:1 H2O
  6. customThe crystals were then dried overnight in a vacuum oven at 50° C

Sources & evidence

ORD record
ord-4fa8ef48f1144f928523ac509f49b51e
Source dataset
uspto-grants-1987_05
Patent number
US04665097

Reaction notes

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