Methane, dichloromethoxy- → 3-(o-Carbomethoxypheylthio-)4-methoxybenzaldehyde

HRID 1380562Notes

Reaction equation

HRID 1380562 reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[S:9][C:10]1[CH:19]=[CH:18][CH:17]=[CH:16][C:11]=1[C:12]([O:14][CH3:15])=[O:13].[CH3:20][O:21]C(Cl)Cl>ClCCCl.[Ti](Cl)(Cl)(Cl)Cl>[C:12]([C:11]1[CH:16]=[CH:17][CH:18]=[CH:19][C:10]=1[S:9][C:4]1[CH:5]=[C:6]([CH:7]=[CH:8][C:3]=1[O:2][CH3:1])[CH:20]=[O:21])([O:14][CH3:15])=[O:13]

Participants

5

Procedure

Dissolve 117 g (0.427 mole) of the ester of Step B in 1500 ml of 1,2-dichloroethane and cool with stirring in an ice-bath. Add 200 ml (345 g, 1.82 mole) of titanium tetrachloride at a rapid dropwise rate. Add also fairly rapidly 154 g (1.34 mole) of dichloromethyl methyl ether. Stir the mixture under a nitrogen atmosphere overnight then pour into ice. After shaking, separate the organic phase and extract the aqueous phase twice with methylene chloride. Wash the combined organic phases twice with water, dry and strip to an oil which crystallizes. (m.p. 99°-104° C.).

Workup

  1. temperaturecool
  2. stirringStir the mixture under a nitrogen atmosphere overnight
  3. additionthen pour into ice
  4. stirringAfter shaking
  5. customseparate the organic phase
  6. extractionextract the aqueous phase twice with methylene chloride
  7. washWash the combined organic phases twice with water
  8. customdry
  9. customstrip to an oil which crystallizes

Sources & evidence

ORD record
ord-76087fd58cd0437a810d464a02d9fdc8
Source dataset
uspto-grants-1986_04
Patent number
US04582842

Reaction notes

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