1,2-Dichloroethane → HCID 20506436, compound

HRID 1703378Notes

Reaction equation

HRID 1703378 reaction equation
[NH2:1][C:2]1[C:7]([C:8]#[N:9])=[CH:6][C:5]([Cl:10])=[C:4]([O:11][CH3:12])[CH:3]=1.ClCCCl.[C:17](Cl)(Cl)=[S:18].C(=O)([O-])[O-].[Ca+2]>O>[Cl:10][C:5]1[CH:6]=[C:7]([C:2]([N:1]=[C:17]=[S:18])=[CH:3][C:4]=1[O:11][CH3:12])[C:8]#[N:9]

Participants

6

Reactant 4

HCID 111,2-Dichloroethane2×HCID 10040ThiophosgeneHCID 10112Calcium CarbonateHCID 20506454HCID 20506454, compound

Product 1

HCID 20506436HCID 20506436, compound

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Conditions

Temperature
20 °C

Procedure

To a solution of 27.4 g. (0.15 mole) of 6-amino-3-chloro-4-methoxybenzonitrile in 150 ml. of 1,2-dichloro-ethane at 0°-5° C. is added with stirring a mixture of 23 g. (0.2 mole) thiophosgene, 100 ml. 1,2-dichloroethane, 20 g. (0.2 mole) calcium carbonate and 200 ml. of water. After the addition the mixture is stirred for one hour at 0°-5° C., warmed to 20° C. and stirred for 6 hours at this temperature and finally at 35° C. for an hour. The reaction mixture is filtered and the organic layer separated, washed with dilute hydrochloric acid, water and dried (MgSO4). The solvent is removed by evaporation and the residue used without purification in the next step.

Workup

  1. additiona mixture of 23 g
  2. additionAfter the addition the mixture
  3. stirringis stirred for one hour at 0°-5° C.
  4. stirringstirred for 6 hours at this temperature and finally at 35° C. for an hour
  5. filtrationThe reaction mixture is filtered
  6. customthe organic layer separated
  7. washwashed with dilute hydrochloric acid, water
  8. dry with materialdried (MgSO4)
  9. customThe solvent is removed by evaporation
  10. customthe residue used without purification in the next step

Sources & evidence

ORD record
ord-f00264946d884b0db041eb265174689a
Source dataset
uspto-grants-1982_09
Patent number
US04351940

Reaction notes

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