Carbon Disulfide → HCID 10990345, compound

HRID 1444821Notes

Reaction equation

HRID 1444821 reaction equation
[H-].[Na+].[P:3]([O-:10])([O:7][CH2:8][CH3:9])[O:4][CH2:5][CH3:6].[H][H].[C:13](=[S:15])=[S:14].[CH2:16](Cl)[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>O1CCCC1.C(OCC)C>[CH2:5]([O:4][P:3]([C:13]([S:15][CH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)=[S:14])([O:7][CH2:8][CH3:9])=[O:10])[CH3:6]

Participants

8

Procedure

To a stirred slurry of sodium hydride (60% dispersion in mineral oil) (8 g, 0.2 mol) in tetrahydrofuran (200 mL) was added diethyl phosphite (27.5 g, 0.2 mol) dropwise under nitrogen. The mixture was stirred until hydrogen evolution ceased (about 15 minutes). The mixture was allowed to cool in an ice-water bath and carbon disulfide (76 g, 1 mol) was added over 15 minutes followed by benzyl chloride (25.2 g, 0.2 mol) in THF (100 mL) over 20 minutes. The resultant mixture was stirred at room temperature for 24 hours. Diethyl ether (200 mL) was added and the mixture washed with water (3×200 mL). The organic layer was dried (MgSO4), filtered and evaporated in vacuo. After column chromatography (Kieselgel-60, 70-230 mesh, 1:4 ethyl acetate/n-hexane eluent), S-benzyl diethoxyphosphinyldithioformate (20) was obtained (11 g, 18% yield) as a red oil. 1H-nmr (CDCl3) d (ppm) 1.43 (t, 6H); 4.38 (s, 2H), 4.65 (q, 4H) and 7.30-7.45 (m, 5H).

Workup

  1. custom(about 15 minutes)
  2. temperatureto cool in an ice-water bath
  3. washthe mixture washed with water (3×200 mL)
  4. dry with materialThe organic layer was dried (MgSO4)
  5. filtrationfiltered
  6. customevaporated in vacuo

Sources & evidence

ORD record
ord-b60d03a4d00d42fbb37fa782f3789f63
Source dataset
uspto-grants-2010_02
Patent number
US07662986B2

Reaction notes

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