Hydrochloric Acid → 4-(Butylsulfanyl)-1-methyl-3,5-diphenyl-1H-pyrazole

HRID 1439136Notes

Reaction equation

HRID 1439136 reaction equation
Br[C:2]1[C:3]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)=[N:4][N:5]([CH3:13])[C:6]=1[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.[CH2:20]([SH:24])[CH2:21][CH2:22][CH3:23].N1C2C(=CC=CC=2)C=CC=1.Cl>N1C=CC=CC=1>[CH2:20]([S:24][C:2]1[C:3]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)=[N:4][N:5]([CH3:13])[C:6]=1[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)[CH2:21][CH2:22][CH3:23]

Participants

6

Reactant 4

HCID 313Hydrochloric AcidHCID 7047QuinolineHCID 8012ButanethiolHCID 213980514-Bromo-1-methyl-3,5-diphenyl-1H-pyrazole

Product 1

HCID 213980704-(Butylsulfanyl)-1-methyl-3,5-diphenyl-1H-pyrazoleYield 97.1%

Reagents, catalysts & solvents 1

HCID 1049PyridineSolvent

Procedure

A mixture of 4-bromo-1-methyl-3,5-diphenylpyrazole (21 g, 0.0671 mole), copper(1)salt of butanethiol (12.58 g, 0.08 mole), pyridine (10 ml) and quinoline (100 ml) is stirred and heated at 175° C to 180° C for 8 hours. The reaction mixture is cooled, poured into dilute hydrochloric acid (500 ml) and extracted with benzene. The benzene layer is separated and stripped in vacuo to give a brown oil. The oil is slurried with petroleum ether (b.p. 40° C to 60° C), filtered and the filtrate stripped in vacuo to give a brown syrup 21 g (97%), >95% pure by glc.

Workup

  1. temperatureheated at 175° C to 180° C for 8 hours
  2. temperatureThe reaction mixture is cooled
  3. extractionextracted with benzene
  4. customThe benzene layer is separated
  5. customto give a brown oil
  6. filtrationfiltered

Sources & evidence

ORD record
ord-c4d8106b090b4635b1c569efd9022d38
Source dataset
uspto-grants-1977_11
Patent number
US04058391

Reaction notes

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