1-Octadecene → HCID 178443003, compound

HRID 1589711Notes

Reaction equation

HRID 1589711 reaction equation
[CH2:1]=[CH:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18].[S:19][Cl:20]>>[CH3:18][CH2:17][CH2:16][CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH:2]=[CH2:1].[S:19][Cl:20]

Participants

3

Reactant 2

HCID 82171-OctadeceneHCID 15930840CID 15930840

Product 1

HCID 178443003HCID 178443003, compound

Procedure

Approximately 840 gm (3.0 mol. 90% purity) of octadecene was charged into a 2-liter reactor equipped with dropping funnel, reflux condenser, thermometer, and mechanical stirrer. Approximately 202.5 gm (1.5 mol.) of sulfur monochloride was added through the dropping funnel. Then the reaction mixture was heated to 95° to 100° C. to activate the sulfochlorination reaction. Moderate exotherm brought the temperature to 113° C. then the reaction was held at 110° C. for four hours. Near the end of the period at 110° C., the color became dark reddish. At completion, the product was left to cool slowly. This produced approximately 103 gm liquid material (C36H72S2Cl2).

Workup

  1. customequipped
  2. temperaturereflux condenser
  3. temperatureThen the reaction mixture was heated to 95° to 100° C.
  4. customthe sulfochlorination reaction
  5. customto 113° C.
  6. customat 110° C.
  7. waitAt completion, the product was left
  8. temperatureto cool slowly

Sources & evidence

ORD record
ord-4dbd8aba6979441681eddde33520ccf8
Source dataset
uspto-grants-1993_04
Patent number
US05199960

Reaction notes

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