HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → tert-butyl 3-[(1S)-1-hydroxypropyl]benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Tert-butyl 3-formylbenzoate | HCID 10845940 | — |
| Reactant | (1S,2R)-(-)-2-(Dibutylamino)-1-phenyl-1-propanol | HCID 11003877 | — |
| Reactant | HCID 178418750 | HCID 178418750 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | tert-butyl 3-[(1S)-1-hydroxypropyl]benzoate | HCID 66934833 | 1,950.8% |
Reaction Steps
To the (1S,2R)-2-di-n-butylamino-1-phenyl-1-propanol (200 mg) in toluene (7 ml) solution, tert-butyl 3-formylbenzoate (3 g) in hexane (7 ml) solution was added and the mixture was stirred at room temperature for 20 minutes. Next, diethylzinc in 1N hexane solution (33 ml) was added to the reaction solution under ice cooling and the mixture was stirred at that temperature for 18 hours. Saturated ammonium chloride aqueous solution was added to the reaction solution, the mixture was stirred at 20 minutes, and 1N hydrochloric acid was added. The obtained mixed solution was extracted with ethyl acetate. The organic layer was dried over with anhydrous sodium sulfate, then concentrated to obtain the title compound (3.5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08507714B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-1ae8f9d9b0f84ee3b80db555bfaf0f42 |
| Source note | uspto-grants-2013_08 |