Reacción #2487412

ord-b11fbe60f5c048cd843060f2395c5889

Ecuación de reacción

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

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroequipped with a stirrer
  2. 2
    Extracciónextracting with diethyl ether
  3. 3
    LavadoThe ether phase was washed three times with water
  4. 4
    Secadodried over sodium sulphate
  5. 5
    Otrobefore finally removing the diethyl ether
  6. 6
    Otroby evaporation
  7. 7
    OtroThe residue was recrystallised three times from methanol
  8. 8
    Otrogiving a yield of 2.6 grams (83%)

Procedimiento

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).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08795782B2uspto-grants-2014_08