Hydrochloric Acid → HCID 178447890, compound

HRID 635120Notes

Reaction equation

HRID 635120 reaction equation
[Mg].[CH2:2]([C@H:5]1[CH2:10][CH2:9][C@H:8]([C:11]2[CH:16]=[CH:15][C:14](Br)=[CH:13][CH:12]=2)[CH2:7][CH2:6]1)[CH2:3][CH3:4].[C:18](=[S:20])=[S:19].Cl>C1COCC1>[CH2:2]([C@H:5]1[CH2:10][CH2:9][C@H:8]([C:11]2[CH:16]=[CH:15][C:14]([C:18]([SH:20])=[S:19])=[CH:13][CH:12]=2)[CH2:7][CH2:6]1)[CH2:3][CH3:4]

Participants

6

Reactant 4

HCID 313Hydrochloric AcidHCID 6348Carbon DisulfideHCID 5462224MagnesiumHCID 178447827HCID 178447827, compound

Product 1

HCID 178447890HCID 178447890, compoundYield 17.7%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent2×

Procedure

To a solution obtained by suspending 2.25 g (93 mmol) of magnesium in 50 mL of THF, a solution of 20.0 g (71 mmol) of 4-(trans-4-propylcyclohexyl)phenyl bromide in 100 mL of THF was added dropwise with stirring at the room temperature for 45 minutes and stirred with reflux for 30 minutes, to prepare a Grignard reagent. To the solution, 16.3 g (214 mmol) of carbon disulfide was added dropwise for 15 minutes at the room temperature and stirred for one night. To the reaction solution, 60 mL of 3M hydrochloric acid was added to stop the reaction, extracted with ether, and dried with anhydrous magnesium sulfate. After filtering off magnesium sulfate, the filtrate was concentrated under reduced pressure, to obtain 3.5 g (yield 17.7%) of 4-(trans-4-propylcyclohexy)phenyl dithiocarboxylic acid.

Workup

  1. customTo a solution obtained
  2. stirringstirred
  3. temperaturewith reflux for 30 minutes
  4. stirringstirred for one night
  5. customthe reaction
  6. extractionextracted with ether
  7. dry with materialdried with anhydrous magnesium sulfate
  8. filtrationAfter filtering off magnesium sulfate
  9. concentrationthe filtrate was concentrated under reduced pressure

Sources & evidence

ORD record
ord-8755402cde5a48ba8ceeb84509e79184
Source dataset
uspto-grants-2001_02
Patent number
US06187223B1

Reaction notes

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