HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 5-(4-Cyanophenyl)-3-hydroxymethyl-1,2,4-oxadiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-Ethoxycarbonyl-5-(4-cyanophenyl)-1,2,4-oxadiazole | HCID 19959148 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-(4-Cyanophenyl)-3-hydroxymethyl-1,2,4-oxadiazole | HCID 19959169 | 96.7% |
Reaction Steps
To a solution of 5-(4-cyanophenyl)-3-ethoxycarbonyl-1,2,4-oxadiazole (5.0 g) in methanol (50 ml)--tetrahydrofuran (50 ml) was added sodium borohydride (0.93 g) at 0° C. After stirring at 5°-10° C. for 1 hour, the mixture was poured into water and extracted with ethyl acetate. The extract was washed with water and brine, dried over magnesium sulfate, and evaporated in vacuo. The residue was recrystallized from diethyl ether to give 5-(4-cyanophenyl)-3-hydroxymethyl-1,2,4-oxadiazole (4.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05622976 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-008dbd1864a042c18c6448049da19547 |
| Source note | uspto-grants-1997_04 |