HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Benzophenone O-[(R)-3-pyrrolidinyl]oxime
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzophenone oxime | HCID 11324 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | N-tert-butoxy-carbonyl-3-(S)-pyrrolidinyl methanesulfonate | HCID 86649201 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | Benzophenone O-[(R)-3-pyrrolidinyl]oxime | HCID 86635562 | — |
Reaction Steps
To a suspension of KOH powder (4.86 g) in DMSO (250 ml) under vigorous stirring, benzophenone oxime (7.86 g) was added. After stirring at RT for 30 min, a solution of N-tert-butoxy-carbonyl-3-(S)-pyrrolidinyl methanesulfonate (10.0 g) in DMSO (70 ml) was added. After 18 h at RT the reaction was poured into iced water (900 ml) and extracted with Et2O. The combined organic layers were washed with water, brine, dried and the solvent was evaporated. Benzophenone O-[(R)-3-pyrrolidinyl]oxime was obtained (13.0 g, 96%) as a white solid and used without any further purification in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08664210B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-f8f665f9d95d4dd090525fd18558d9b0 |
| Source note | uspto-grants-2014_03 |