Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 22000240 | HCID 22000240 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 22000239 | HCID 22000239 | 54% |
Reaction Steps
A solution of 1-(3-cyanophenyl)-3-pyrrolidinol (0.65 g, 4.1 mmol) in triethyl amine (5.72 ml, 41 mmol) and DMSO (15 ml) was cooled to 0° C. and pyridine-SO3 (1.96 g, 12.3 mmol) was added. The mixture was stirred at 0° C. for 1 hr and at room temperature for 18 hr. The reaction mixture was poured into water (100 ml) and extracted three times with methylene chloride. The methylene chloride extracts were dried over magnesium sulfate and concentrated in vacuo to give 1-(3-cyanophenyl)-3-pyrrolidinone (0.41 g, 54%) that was used without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06225324B1 |
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| Source dataset | uspto-grants-2001_05 |
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| ORD ID | ord-abe389567f61407bbfb7b3ebba462d12 |
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| Source note | uspto-grants-2001_05 |
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