HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2,2-dimethyl-4-[N-(beta-trimethylsilylethanesulfonyl)-aminomethyl]-1,3-dioxolane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,3-Dioxolane-4-methanamine, 2,2-dimethyl- | HCID 4122349 | — |
| Reactant | 2-(Trimethylsilyl)ethane-1-sulfonyl chloride | HCID 9837086 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2,2-dimethyl-4-[N-(beta-trimethylsilylethanesulfonyl)-aminomethyl]-1,3-dioxolane | HCID 19426282 | — |
Reaction Steps
A solution of 2,2-dimethyl-4-aminomethyl-1,3-dioxolane (10.0 g, 0.08 mol) and triethylamine (8.1 g, 11.1 mL, 0.08 mol) in 100 mL of N,N-dimethylformamide is cooled to 0 C. under argon atmosphere. Then β-trimethylsilylethanesulfonyl chloride (16.0 g, 0.08 mol) is added dropwise. The solution is allowed to reach 25 C. and is stirred for 15 hours. The solvents are removed under reduced pressure and the crude residue is partitioned between dichloromethane (100 mL) and 5% sodium bicarbonate solution (50 mL). The layers are separated and the organic layer is dried over anhydrous sodium sulfate and evaporated to give 2,2-dimethyl-4-[N-(β-trimethylsilylethanesulfonyl)-aminomethyl]-1,3-dioxolane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05554749 |
| Source dataset | uspto-grants-1996_09 |
| ORD ID | ord-4b2911baafe14fc485e2830d527b10aa |
| Source note | uspto-grants-1996_09 |