HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 10714242, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butyldiphenylchlorosilane | HCID 94078 | — |
| Reactant | (R)-Solketal | HCID 736056 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10714242 | HCID 10714242 | 106.2% |
Reaction Steps
To a solution of ((4R)-2,2-dimethyl-1,3-dioxolan-4-yl)methan-1-ol (9 g, 68.6 mmol) in anhydrous dichloromethane (40 mL) were added triethylamine (11.2 mL), tert-butylchlorodiphenylsilane (19.8 g, 372 mmol), and N,N-dimethylaminopyridine (DMAP, 418 mg, 3.4 mmol) at room temperature under a nitrogen atmosphere. The reaction mixture was stirred at room temperature overnight. It was then diluted with additional dichloromethane and the reaction mixture was washed with water, brine, dried over sodium sulfate, filtered and evaporated to give the title compound (27 g) which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07163958B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-20fcae362223490bb58a1c5c72e39418 |
| Source note | uspto-grants-2007_01 |