Triisopropyl phosphite → HCID 21255885, compound
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]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 2
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
- filtrationThe mixture was then filtered
- customthe filtrate was partitioned
- extractionThe aqueous layer was further extracted with dichloromethane (2×)
- washthe combined extracts were washed with brine (1×)
- customdried
- concentrationconcentrated
- 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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