Reaction #2487412

ord-b11fbe60f5c048cd843060f2395c5889

Reaction equation

O
water
CCN(CC)C(=S)[S-].O.O.O.[Na+]
sodium diethyldithiocarbamate trihydrate
C=Cc1ccc(CCl)cc1
4-vinylbenzyl chloride
C=Cc1ccc(SC(=S)N(CC)CC)cc1
Diethyl-Dithiocarbamic Acid 4-Vinyl-Phenyl Ester

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Otherequipped with a stirrer
  2. 2
    Extractionextracting with diethyl ether
  3. 3
    WashThe ether phase was washed three times with water
  4. 4
    Dryingdried over sodium sulphate
  5. 5
    Otherbefore finally removing the diethyl ether
  6. 6
    Otherby evaporation
  7. 7
    OtherThe residue was recrystallised three times from methanol
  8. 8
    Othergiving a yield of 2.6 grams (83%)

Procedure

A solution of sodium diethyldithiocarbamate trihydrate (3.5 g, 1.55×10−2 mol) in 20 mL of ethanol was added to a flask equipped with a stirrer, dropping funnel and a reflux condenser. To this solution was added a solution of 4-vinylbenzyl chloride (3.0 g, 1.96×10−2 mol) and ethanol (5 mL), dropwise, over a period of 0.5 h at a temperature of 0° C. The resultant solution was stirred at room temperature for 24 h before pouring into a large volume of water and extracting with diethyl ether. The ether phase was washed three times with water, dried over sodium sulphate, before finally removing the diethyl ether by evaporation. The residue was recrystallised three times from methanol, giving a yield of 2.6 grams (83%). 1H NMR (CDCl3) δ7.36 (s, 4H, C6H4), 6.70 (dd, J=11.6 and 17.5 Hz, 1H, CH═CH2), 5.73 (d, J=17.5 Hz, 1H, CH═CH2), 5.24 (d, J=11.5 Hz, 1H, CH═CH2), 4.54 (s, 2H, CH2S), 4.04 (q, J=7.3 Hz, 2H, NCH2), 3.73 (q, J=6.6 Hz, 2H NCH2), 1.19 (t, J=ca.7.0 Hz, 6H CH2CH3).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08795782B2uspto-grants-2014_08