1,3-Propanedithiol → 2-Methyl-2-dichloromethyl-1,3-dithiane

HRID 1743279Notes

Reaction equation

HRID 1743279 reaction equation
[Cl:1][CH:2]([Cl:6])[C:3]([CH3:5])=O.[CH2:7]([SH:11])[CH2:8][CH2:9][SH:10]>C(Cl)(Cl)Cl>[CH3:5][C:3]1([CH:2]([Cl:6])[Cl:1])[S:11][CH2:7][CH2:8][CH2:9][S:10]1

Participants

4

Conditions

Temperature
0 °C

Procedure

In a three-necked flask equipped with a magnetic stirrer and having a nitrogen blanket at the inlet and outlet, are added 13.97 grams (0.11 mole) of 1,1-dichloroacetone, 10.8 grams (0.10 mole) of 1,3-propanedithiol and 50 milliliters of chloroform. The reaction mixture is cooled to 0° C. A slow steam of hydrogen chloride gas is then bubbled through the solution for approximately five minutes. Upon the reaction mixture reaching saturation, the mixture is allowed to set at room temperature for approximately thirty minutes. The solvent is then evaporated and a crude 2-methyl-2-dichloromethyl-1,3-dithiane derivative is expected in a yield of approximately 80–90%.

Workup

  1. customIn a three-necked flask equipped with a magnetic stirrer
  2. customA slow steam of hydrogen chloride gas is then bubbled through the solution for approximately five minutes
  3. waitto set at room temperature for approximately thirty minutes
  4. customThe solvent is then evaporated

Sources & evidence

ORD record
ord-4e25cd6bdea94771b05d17ab1b060a9a
Source dataset
uspto-grants-2006_03
Patent number
US07009032B2

Reaction notes

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