HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,2,7,7-Tetramethyl-3,6-dioxa-2,7-disilaoctane → HCID 14638051, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,2,7,7-Tetramethyl-3,6-dioxa-2,7-disilaoctane | HCID 81858 | — |
| Reactant | 4,4-Dimethyl-5-nitropentan-2-one | HCID 4156383 | — |
| Catalyst | Trimethylsilyl triflate | HCID 65367 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 14638051 | HCID 14638051 | 97.2% |
Reaction Steps
A stirred solution of 1,2-bis(trimethylsilyloxy)ethane (26.5 g, 128 mmol) in dichloromethane (50 mL) was cooled in a dry ice/isopropanol bath, and trimethylsilyl trifluoromethanesulfonate (2.2 g, 1.0 mmol) was added, followed by the dichloromethane solution of 4,4-dimethyl-5-nitropentan-2-one (50 mL, 19.0 g, 119 mmol) from the previous step. After 30 minutes, the cooling bath was removed and the solution was allowed to warm to room temperature. The solution was filtered through a plug of potassium carbonate and concentrated under reduced pressure to provide 2-(2,2-dimethyl-3-nitropropyl)-2-methyl-[1,3]dioxolane (23.5 g) as a dark oil that was used directly in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08778963B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-1abb75676dc946808f76058154f87456 |
| Source note | uspto-grants-2014_07 |