HuagongsheHuagongshe Chemistry Print Report · For research reference only
Urea → Benzyl 2-((1-chlorosilolan-1-yl)oxy)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Urea | HCID 1176 | — |
| Reactant | Silacyclopentane, 1,1-dichloro- | HCID 75474 | — |
| Reactant | Benzyl 2-hydroxyacetate | HCID 561337 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Benzyl 2-((1-chlorosilolan-1-yl)oxy)acetate | HCID 90418649 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a solution of cyclotetramethylenedichlorosilane (0.5 mL; 3.82 mMol) in dry THF (5 mL) was added urea (0.275 g; 4.58 mmol). The mixture was then cooled to 0° C. and benzyl glycolate (0.54 mL; 3.82 mmol) was then added dropwise over a 7 minute span. The mixture was then taken off the ice bath and allowed to stir at room temperature for 1 hour. The biphasic mixture was then concentrated under high vacuum and diluted with chloroform. The aqueous layer was then soaked up with excess Na2SO4 and the mixture was filtered. The filtrate was concentrated to a light yellow crude liquid which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09352049B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-2e2b90b4d392470fa201c8d4c458c7f3 |
| Source note | uspto-grants-2016_05 |