Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | CID 53628100 | HCID 178418400 | — |
| Reactant | HCID 178419396 | HCID 178419396 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(4-Aminophenyl)propan-2-ol | HCID 9543261 | 55.9% |
Reaction Steps
To a −78° C. solution of compound 134 (1 g, 3.95 mmol) in ether (20 mL) was added sec-BuLi (1.4 M in hexanes, 0.62 g, 9.67 mmol). The resulting solution was stirred for 30 min at −78° C., followed by addition of acetone (0.91 g, 15.81 mmol) dropwise at −78° C. The reaction mixture was warmed to room temperature overnight. The reaction mixture was partitioned between water and ether and the layers were separated. The aqueous layer was re-extracted with ether. The ether layers were the combined and concentrated in vacuo to yield crude 135 (0.33 g, 55.9%) which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08178542B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-0059d9f2ce044afc99be9811c9af1f91 |
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| Source note | uspto-grants-2012_05 |
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