HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium borohydride → [2-(3-Chloro-phenyl)-2H-tetrazol-5-yl]-methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | HCID 59424218 | HCID 59424218 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [2-(3-Chloro-phenyl)-2H-tetrazol-5-yl]-methanol | HCID 59424225 | 106.2% |
Reaction Steps
2-(3-Chloro-phenyl)-2H-tetrazole-5-carbaldehyde (70.8 mg, 0.339 mmol) was dissolved in THF (5 mL) and lithium borohydride (25.9 mg, 1.187 mmol) was added. The reaction was allowed to reflux under argon for three hours and was then allowed to stir overnight at room temperature. The reaction was quenched with 1M hydrochloric acid and an aqueous workup was done extracting with ethyl acetate three times. The combined organic layers were washed with brine, dried over sodium sulfate, filtered and concentrated to yield the title compound as a white solid (75.8 mg, 106%). 1H NMR (CDCl3) δ (ppm): 8.190 (s, 1H), 8.070 (m, 1H), 7.507 (m, 2H), 5.082 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07691892B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-8a645396c3264dd39f3396c13bc7fbeb |
| Source note | uspto-grants-2010_04 |