HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 19861148, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 19861150 | HCID 19861150 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 19861148 | HCID 19861148 | 80% |
Reaction Steps
Sodium borohydride (0.42 g) was added in small portions to 2-(1,2,4-triazol-1-yl)-2-(2', 4'-dichlorobenzyl)-4'-chloroacetophenone (4.2 g) in methanol (40 ml). When the effervescence ceased, the mixture was refluxed for 1 hour, cooled to room temperature and the methanol removed at the water pump. The residue was acidified with 1N-hydrochloric acid to give a solid which was filtered and washed. Recrystallisation from ethanol/water gave white crystals of the title compound (yield 80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04620011 |
| Source dataset | uspto-grants-1986_10 |
| ORD ID | ord-0f29d682189d44a2bd09356ca195671d |
| Source note | uspto-grants-1986_10 |