HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → (R)-beta-aminophenethyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Phenylglycine, D- | HCID 70134 | — |
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (R)-beta-aminophenethyl alcohol | HCID 2724025 | — |
Reaction Steps
20 g (920 mmol) of lithium borohydride are dissolved in 420 ml of absolute tetrahydrofuran. 233.5 ml (1.84 mol) of trimethylchlorosilane are added dropwise, while stirring, and 69.5 g (0.46 mol) of (R)-phenylglycine are then added in portions within the space of 4 hours. The reaction mixture is stirred at room temperature overnight. 690 ml of methanol are then added and the mixture is stirred at room temperature for 2 hours and concentrated in vacuo. The residue is dissolved, while stirring, in 690 ml of a 20% aqueous solution of potassium hydroxide. The aqueous phase is extracted three times with ethyl acetate. The combined organic phases are washed with water, dried over magnesium sulphate and concentrated in vacuo.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05981492 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-62bef2d833174e03baf16a0eb74b762d |
| Source note | uspto-grants-1999_11 |