HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 13690970, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 13690942 | HCID 13690942 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13690970 | HCID 13690970 | 96.5% |
Reaction Steps
To a solution of 1.03 g of 5-[3-(4-biphenylyl)-3-oxopropyl]-3-chloromethyl-1,2,4-oxadiazole obtained in Example 3 in 100 ml of ethanol was added 0.12 g of sodium borohydride. After stirring for 10 minutes at room temperature, the reaction mixture was concentrated under reduced pressure. The residue was treated with ice-water and extracted with chloroform. The organic phase was washed with water, dried over sodium sulfate and evaporated to give 1.0 g of 5-[3-(4-biphenylyl)-3-hydroxypropyl]-3-chloromethyl-1,2,4-oxadiazole, m.p. 48°-49° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04618617 |
| Source dataset | uspto-grants-1986_10 |
| ORD ID | ord-56ed1a60574d40b594c2d97844036044 |
| Source note | uspto-grants-1986_10 |