HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium borohydride → HCID 21709156, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | 4-Pyrimidinecarbonyl chloride, 2-phenyl- | HCID 54128884 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 21709156 | HCID 21709156 | 81% |
Reaction Steps
To a solution of 145 mg of 2-phenyl-4-pyrimidinecarboxylic acid chloride in 5 mL tetrahydrofuran was added excess lithium borohydride. The reaction mixture was stirred at room temperature for 10 minutes then diluted with 25 mL of ethyl acetate and filtered. The filtrate was washed successively with 25 mL aliquots of 1 N sodium hydroxide and brine. The solvent was removed by evaporation under reduced pressure to yield 100 mg of 2-phenyl-4-hydroxymethylpyrimidine as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06221871B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-42b6410450854cf5964f5f4bbebb3b3b |
| Source note | uspto-grants-2001_04 |