Sodium Cyanide → HCID 22907086, compound

HRID 1720597Notes

Reaction equation

HRID 1720597 reaction equation
[S:1]1[CH2:6][CH2:5][C:4](=O)[CH2:3][CH2:2]1.[C-:8]#[N:9].[Na+].[Cl-:11].[NH4+:12].C(=O)([O-])[O-].[K+].[K+]>CO.O>[ClH:11].[NH2:12][C:4]1([C:8]#[N:9])[CH2:5][CH2:6][S:1][CH2:2][CH2:3]1

Participants

7

Reactant 4

HCID 8929Sodium CyanideHCID 11430Potassium CarbonateHCID 25517Ammonium ChlorideHCID 66173Tetrahydrothiopyran-4-one

Product 1

HCID 22907086HCID 22907086, compound

Reagents, catalysts & solvents 2

HCID 887MethanolSolventHCID 962WaterSolvent2×

Procedure

A solution of tetrahydrothiopyran-4-one (4.64 g, 40.0 mmol) in methanol (10 mL) is added to a mixture of sodium cyanide (2.0 g, 40.0 mmol) and ammonium chloride (2.36 g, 44.0 mmol) in water (8 mL). The reaction mixture is heated to reflux for 14 hours. The mixture is diluted with water, basified with potassium carbonate, and extracted with diethyl ether. The organic extract is dried (MgSO4) and filtered. The solution is acidified with hydrochloric acid saturated with methylene chloride. The resulting precipitate is filtered off providing 4-amino-4-cyano-tetrahydrothiopyran hydrochloride salt.

Workup

  1. temperatureThe reaction mixture is heated
  2. temperatureto reflux for 14 hours
  3. extractionextracted with diethyl ether
  4. extractionThe organic extract
  5. dry with materialis dried (MgSO4)
  6. filtrationfiltered
  7. filtrationThe resulting precipitate is filtered off

Sources & evidence

ORD record
ord-c984a7b95ab94bdaa1121b6495038dcb
Source dataset
uspto-grants-1996_04
Patent number
US05506242

Reaction notes

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