HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium borohydride → HCID 178447299, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | HCID 178447304 | HCID 178447304 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178447299 | HCID 178447299 | — |
Reaction Steps
0.8 g of N-valeryl-N-[(2'-(1H-tetrazol-5-yl)biphenyl-4-yl)methyl]-(L)-valine methyl ester is dissolved in 30 ml of THF, treated at 5° C. with 83 mg of lithium borohydride and stirred at room temperature for 24 h. The reaction mixture is then concentrated, treated with water and adjusted to pH 2 with hydrochloric acid, a white precipitate forming. The mixture is extracted with ethyl acetate, washed with water and brine, dried and finally separated by means of flash chromatography (CH2Cl2 -MeOH 5:1). FAB-MS: m/e=422 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05399578 |
| Source dataset | uspto-grants-1995_03 |
| ORD ID | ord-5ab661b10dc244f09f1445c57d533084 |
| Source note | uspto-grants-1995_03 |