HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → (S)-3-((tert-Butyldimethylsilyl)oxy)pyrrolidin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | (3S)-3-hydroxypyrrolidin-2-one | HCID 11029774 | — |
| Solvent | Water | HCID 962 | — |
| Product | (S)-3-((tert-Butyldimethylsilyl)oxy)pyrrolidin-2-one | HCID 10584804 | 42.2% |
Reaction Steps
In an ice bath, 570 mg of imidazole and 947 mg of t-butyldimethylsilyl chloride were added to a dimethylformamide (5 ml) solution of 503 mg of (3S)-3-hydroxypyrrolidin-2-one, and stirred at room temperature for 1 hour. Water was added to the reaction liquid, extracted with ethyl acetate, the organic layer was washed with water and saturated saline water, and dried. The solvent was evaporated away under reduced pressure to obtain 452 mg of the entitled compound as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07932394B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-87688e58680947d8998560456a7d42a5 |
| Source note | uspto-grants-2011_04 |