HuagongsheHuagongshe Chemistry Print Report · For research reference only
trans-4-(t-Butyldimethylsilyloxymethyl)-2-(diethyloxyphosphinoyl)-1,3-dithiolane → cis 2-(Diethyloxyphosphinoyl)-4-hydroxymethyl-1,3-dithiolane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | trans-4-(t-Butyldimethylsilyloxymethyl)-2-(diethyloxyphosphinoyl)-1,3-dithiolane | HCID 131720785 | — |
| Catalyst | Acetyl chloride | HCID 6367 | — |
| Catalyst | Ammonium Chloride | HCID 25517 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | cis 2-(Diethyloxyphosphinoyl)-4-hydroxymethyl-1,3-dithiolane | HCID 86752990 | 77.6% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a solution of cis-4-(t-butyldimethylsilyloxymethyl)-2-(diethyloxyphosphinoyl)-1,3-dithiolane (example 49) (3.70 g, 9.56 mmol) in anhydrous methanol (50 mL) was added acetyl chloride (6 drops) at 0° C. The solution was stirred at 0° C. for 30 min and then at room temperature for 4.5 hrs. A saturated solution of ammonium chloride (3 drops) was added and the solution was stirred for 15 min followed by evaporation of solvents. The crude material was purified by flash chromatography with a mixture of dichloromethane and methanol (95:5) to give the compound (2.02 g) in 77% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06194576B1 |
| Source dataset | uspto-grants-2001_02 |
| ORD ID | ord-fb49b28cf0d44aef955dd05f3ca728ca |
| Source note | uspto-grants-2001_02 |