Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | α-Phenyl-2-benzofuranmethanol | HCID 15150176 | — |
| Reactant | HCID 21277788 | HCID 21277788 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 70351161 | HCID 70351161 | — |
Reaction Steps
To 0.08 moles of imidazole in 70 ml of acetonitrile, at the temperature of 10 C., 0.02 moles of thionylchloride are added, followed by 1 hour rest, and then 0.02 moles of (benzofuran-2-yl)phenylmethanol are added in 20 ml of acetonitrile. The reaction admixture is kept 24 hours at ambient temperature and then concentrated to dryness. The residue is taken up with ethylether, washed first with 2% sodium hydrate solution and then with water: the hydrochloride is obtained from the ethereal solutions using 5% hydrochloric acid, then an oil is obtained by alkalinization with 5% NaOH, which is extracted with ethylether. The ethereal extract is washed, made anhydrous and saturated with gaseous HCl: the precipitate thus obtained is crystallized from isopropanol: m.p. 205°-207° C. (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04800208 |
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| Source dataset | uspto-grants-1989_01 |
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| ORD ID | ord-7d1c411564f147e6b827747a4042f182 |
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| Source note | uspto-grants-1989_01 |
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