HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (S)-3-((tert-Butyldimethylsilyl)oxy)pyrrolidin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | (3S)-3-hydroxypyrrolidin-2-one | HCID 11029774 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-3-((tert-Butyldimethylsilyl)oxy)pyrrolidin-2-one | HCID 10584804 | 72.1% |
Reaction Steps
A mixture of 14 g of (S)-3-hydroxy-2-pyrrolidinone, 45 g of tert-butyldimethylsilyl chloride, 50 ml of triethylamine and 500 ml of dichloromethane was stirred overnight. The solution was washed four times with water, once with brine, dried and concentrated in vacuo. The residue was dissolved in 500 ml of methanol, refluxed overnight and concentrated in vacuo. The residue was purified by chromatography (silica gel), giving 21.5 g of (S)-3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-2-pyrrolidinone; [α]D260 =-52° (dichloromethane); mp 48°-49° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04937235 |
| Source dataset | uspto-grants-1990_06 |
| ORD ID | ord-73f887c7df9741d5bf6c52c2c493b25b |
| Source note | uspto-grants-1990_06 |