Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | HCID 68666369 | HCID 68666369 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68666357 | HCID 68666357 | 88.2% |
Reaction Steps
Boron tribromide (10.1 mL, 1.0 M in CH2Cl2, 10.1 mmol) was added dropwise to a solution of trans-5-(4-methoxy-3-methyl-phenyl)-3-(2-propenyl)-2-pyrrolidinone (1.13 g, 4.61 mmol) in 10.0 mL of CH2Cl2 at −78° C. The mixture was stirred at −78° C. for 30 min and then at 0° C. for 1 hr. The reaction was quenched by 20 mL of H2O. The mixture was poured into a mixture of ethyl ether and EtOAc (1:1, 50.0 mL) and extracted with 2.0 N of NaOH (3×30 mL). Aqueous layers were combined and acidified using 5.0 N HCl and extracted with EtOAc (3×50 mL). Organic layers were combined, dried over MgSO4, and concentrated to give 940 mg (88%) of the crude title compound as a light brown solid, which was used for next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07659294B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-54f30841678b4af1ac5ba7d8db2a4987 |
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| Source note | uspto-grants-2010_02 |
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