HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Triphenylphosphoranylidene)acetone → 1-(1-CBZ-2(S)-pyrrolidinyl)-1-buten-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Triphenylphosphoranylidene)acetone | HCID 15038 | — |
| Reactant | (S)-2-Formyl-pyrrolidine-1-carboxylic acid benzyl ester | HCID 11746545 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(1-CBZ-2(S)-pyrrolidinyl)-1-buten-3-one | HCID 57212503 | — |
Reaction Steps
To a 350 mg (1.50 mmol) sample of CBZ-L-prolinal, from step 23b above, dissolved in 5 mL of methylene chloride was added 576 mg of 1-triphenylphosphoranylidene-2-propanone (Aldrich, 1.81 mmol). The reaction was stirred at room temperature for 45 min, then heated at reflux for 1.3 hr. The solution was cooled, and a precipitate formed. The mixture was extracted with methylene chloride (3×10 mL). The combined organics were washed with brine and dried over MgSO4. The residue was chromatographed on silica gel, eluting with 25-35% ether in hexane. The title compound was isolated by removal of solvent (279 mg). Anal. Calcd for C16H19NO3 : C, 70.31; H, 7.01; N, 5.12; Found: C, 70.20; H, 7.02; N, 5.10.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05508418 |
| Source dataset | uspto-grants-1996_04 |
| ORD ID | ord-78bb731f7c6149d9a01c73fdfeabd760 |
| Source note | uspto-grants-1996_04 |