HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 14685621, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-(4-Chloro-2-pyrimidinyl)benzaldehyde | HCID 13590378 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 14685621 | HCID 14685621 | — |
Reaction Steps
A 1.0 g portion of 3-(4-chloro-2-pyrimidinyl)benzaldehyde was dissolved in 230 ml of 2-propanol and 0.32 g of freshly ground sodium borohydride pellets was added. After stirring for 3 hours at 50°-60° C. in a water bath, the excess reducing agent was destroyed with 6N hydrochloric acid. The solution was neutralized with sodium bicarbonate and the mixture concentrated in vacuo. The residue was partitioned between ethyl acetate and water. The organic layer was dried over sodium sulfate and then evaporated, giving 1.1 g of the desired intermediate as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04579848 |
| Source dataset | uspto-grants-1986_04 |
| ORD ID | ord-d725d9425e744f0d9357d97130488c10 |
| Source note | uspto-grants-1986_04 |