Pyridine → HCID 178477247, compound

HRID 638529

Reaction equation

HRID 638529 reaction equation
[CH2:1]([P:3]([Cl:6])([Cl:5])=[S:4])[CH3:2].[CH3:7][CH:8](S)[CH3:9].N1C=CC=CC=1>C(#N)C>[CH2:1]([P:3]([Cl:6])([Cl:5])=[SH:4][CH:8]([CH3:9])[CH3:7])[CH3:2]

Participants

5

Procedure

To a mixture of 326 g (2.0 moles) ethylphosphonothioic dichloride in 500 ml acetonitrile, a mixture of 152.3 g (2.0 moles) 2-propanethiol and 158.2 g (2.0 moles) pyridine were added over a period of 20 minutes. The reaction mixture was stirred overnight at room temperature and then heated at reflux for four hours, resulting in the formation of solids. The reaction mixture was cooled to room temperature and then filtered. The filtrate was combined with 500 ml hexane, washed twice with 75 ml water and then stripped to give 373 g of the aboveidentified product as a yellow oil.

Workup

  1. additionwere added over a period of 20 minutes
  2. temperatureheated
  3. temperatureat reflux for four hours
  4. customresulting in the formation of solids
  5. temperatureThe reaction mixture was cooled to room temperature
  6. filtrationfiltered
  7. washwashed twice with 75 ml water

Sources & evidence

ORD record
ord-f7e6006055e24840b08240d3aeadaf06
Source dataset
uspto-grants-1985_12
Patent number
US04562180

Linked notes

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