HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl orthoformate → 4-t-Butyldimethylsilyloxymethyl-2-ethoxy-1,3-dithiolane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| Reactant | 1-t-BUTYLDIMETHYLSILYLOXY-2,3-DIMERCAPTOPROPANE | HCID 21255839 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-t-Butyldimethylsilyloxymethyl-2-ethoxy-1,3-dithiolane | HCID 21255844 | 94% |
Reaction Steps
To a solution of 1-t-butyldimethylsilyloxy-2,3-dimercaptopropane (example 47) (32.00 g, 134 mmol) in toluene (400 mL) were added triethylorthoformate (29.0 mL, 174 mmol, 1.3 eq) and pyridinium p-toluenesulfonate (200 mg). The solution was strirred at 120°-130° C. for 6 hr then was quenched at room temperature with a solution of saturated sodium bicarbonate. The aqueous phase was extracted with dichloromethane and the organic layer was dried with magnesium sulfate and evaporated under reduced pressure. The crude product was obtained in 94% yield (37.17 g) as a 1:1 mixture and was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05955610 |
| Source dataset | uspto-grants-1999_09 |
| ORD ID | ord-1dbabac3454548b8b8dae6467eda05b1 |
| Source note | uspto-grants-1999_09 |