HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 178433453, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 178470724 | HCID 178470724 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 178433453 | HCID 178433453 | 50.2% |
Reaction Steps
A solution of ethyl (4-hydroxy-2-methylpyrimid-6-yl)acetate (0.38 g.) in isopropanol (10 ml.) was heated under reflux and treated with sodium borohydride (0.2 g.). The mixture was heated under reflux for 4 hours with the addition of two further portions (0.1 g.) of sodium borohydride after 2 and 3 hours. The mixture was evaporated to dryness and the residue was partitioned between water and ether. The aqueous phase was acidifed with HOAc and then extracted with EtOAc in a continuous extractor for 24 hours. The extract was dried and then evaporated to dryness to give 4-hydroxy-6-(2-hydroxyethyl)-2-methylpyrimidine (0.15 g.) which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04463005 |
| Source dataset | uspto-grants-1984_07 |
| ORD ID | ord-a1571b8f536543fda2ecdda17b6f1c01 |
| Source note | uspto-grants-1984_07 |