Triisopropyl phosphite → HCID 21255885, compound

HRID 365791Notes

Reaction equation

HRID 365791 reaction equation
[C:1]([O:9][CH2:10][CH:11]1[S:15][CH2:14][CH:13](OC(OC)=O)[O:12]1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[P:21]([O:30]C(C)C)([O:26][CH:27]([CH3:29])[CH3:28])[O:22][CH:23]([CH3:25])[CH3:24].C([O-])(O)=O.[Na+]>ClCCl.[Ti](Cl)(Cl)(Cl)Cl>[C:1]([O:9][CH2:10][CH:11]1[S:15][CH2:14][CH:13]([P:21]([O:26][CH:27]([CH3:29])[CH3:28])([O:22][CH:23]([CH3:25])[CH3:24])=[O:30])[O:12]1)(=[O:8])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

6

Procedure

To a solution of 2-benzoyloxymethyl-5-(methyloxycarbonyloxy)-1,3-oxathiolane (4.80 g, 16.11 mmol) and triisopropyl phosphite (4.77 ml, 19.33 mmol) in dry dichloromethane (100 ml) at 0° C. was added dropwise titanium tetrachloride (1.77 ml, 16.11 mmol). After 2 h at 0° C., the reaction mixture was allowed to warm to room temperature and stirred overnight. The reaction mixture was then poured into saturated NaHCO3 (100 ml). The mixture was then filtered and the filtrate was partitioned. The aqueous layer was further extracted with dichloromethane (2×) and the combined extracts were washed with brine (1×), dried and concentrated. Chromatography eluting with 25-50% EtAc in hexanes yielded the title compound as a 1:1 cis trans mixture (4.958 g, 79%).

Workup

  1. filtrationThe mixture was then filtered
  2. customthe filtrate was partitioned
  3. extractionThe aqueous layer was further extracted with dichloromethane (2×)
  4. washthe combined extracts were washed with brine (1×)
  5. customdried
  6. concentrationconcentrated
  7. washChromatography eluting with 25-50% EtAc in hexanes

Sources & evidence

ORD record
ord-cbfc1ce237b245b9a543106658ea867b
Source dataset
uspto-grants-2000_10
Patent number
US06127540

Reaction notes

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