HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 20559413, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 20492177 | HCID 20492177 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 20559413 | HCID 20559413 | — |
Reaction Steps
Sodium borohydride (165 mg) was added in portions over a period of 10 mins to a solution of 2-[2-[(5-formyl-2-furanylmethyl)thio]ethyl]-1H-isoindole-1,3(2H)-dione (5.0 g) in methanol (100 ml) at 0° C. After stirring for 45 mins, acetic acid (1 ml) was added and the mixture evaporated. Water (100 ml) was added and the solid that precipitated extracted into ethyl acetate (2×150 ml). The ethyl acetate extracts were dried (magnesium sulphate) and evaporated yielding an oil which solidified on trituration in light petroleum (b.p. 60°-80° C.). Crystallisation from methyl acetate-light petroleum (b.p. 60°-80° C.) afforded the title compound as a light, white solid (4.05 g) m.p. 82.5°-84° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04279911 |
| Source dataset | uspto-grants-1981_07 |
| ORD ID | ord-1459e086fe1545369201612e8f7225c5 |
| Source note | uspto-grants-1981_07 |