Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropylamine | HCID 6363 | — |
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | 2-Acetyl-7-hydroxybenzofuran | HCID 595329 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Befunolol | HCID 2309 | — |
Reaction Steps
A mixture of 214 mg. of potassium salt of 2-acetyl-7-hydroxybenzofuran, 70 mg. of isopropylamine and 0.8 ml. of epichlorohydrin was suspended into 5 ml. of ethanol. After heating the suspension in a sealed tube at 100° C. for 20 hours, the reaction mixture was filtered and then the solvent was evaporated under a reduced pressure. The residue was subjected to thin layer chromatography (solid support: Kieselgel PF254 made by E. Merck, developer: benzene-chloroform-methanol-28 % aqueous ammonia (17:4:3:0.4), eluant: chloroform) for the purification to give 2-acetyl-7-(2-hydroxy-3-isopropylaminopropoxy)benzofuran having a melting point of 115° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04056626 |
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| Source dataset | uspto-grants-1977_11 |
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| ORD ID | ord-2f4dc320e8ec472aa9b6bfc8e0bbd185 |
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| Source note | uspto-grants-1977_11 |
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