Reaction #640580

ord-a884f5dc890a4740bf34e54d2f5ea035

Reaction equation

O
water
CCN(CC)CC
triethylamine
S=C(Cl)Cl
thiophosgene
CC(C)(CO)CNCc1ccccc1[N+](=O)[O-]
2,2-Dimethyl-3-(2-nitrobenzylamino)-1-propanol
CC1(C)COC(=S)N(Cc2ccccc2[N+](=O)[O-])C1
5,5-dimethyl-3-(2-nitrobenzyl)-[1,3]-oxazinan-2-thione
Yield 88.8%

Solvents

Conditions

Temperature
0°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    workup.STIRRINGstirred at room temperature for one hour
  2. 2
    Extractionextracted with ethyl acetate
  3. 3
    WashThe organic layer was washed with a saturated brine
  4. 4
    Dryingdried over anhydrous sodium sulfate
  5. 5
    Otherthe solvent was evaporated under reduced pressure
  6. 6
    OtherThe residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:1)

Procedure

2,2-Dimethyl-3-(2-nitrobenzylamino)-1-propanol (1.07 g, 4.50 mmol) was dissolved in chloroform (20 ml) and the reaction solution was cooled to 0° C. Then triethylamine (1.82 g, 18.0 mmol), thiophosgene (0.52 g, 4.50 mmol) was added thereto and stirred at a temperature as is for two hours and at room temperature for one hour. The reaction mixture was added with water, stirred at room temperature for one hour and then extracted with ethyl acetate. The organic layer was washed with a saturated brine and then dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:1) to obtain 5,5-dimethyl-3-(2-nitrobenzyl)-[1,3]-oxazinan-2-thione (1.12 g).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08048825B2uspto-grants-2011_11