HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → Ethylacetate heptane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-[(E)-3-(5-tert-Butyl-6-isobutoxy-4'-methyl-3-biphenylyl)-3-oxopropenyl]benzoic Acid | HCID 12084825 | — |
| Reactant | Cerium trichloride heptahydrate | HCID 21585214 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Ethylacetate heptane | HCID 21899848 | 212.4% |
Reaction Steps
440 mg (0.9 mmol) of 4-[(E)-3-(5-tert-butyl-6-isobutoxy-4′-methyl-3-biphenylyl)-3-oxopropenyl]benzoic acid are dissolved in 50 mL of methanol. 450 mg (1.2 mmol) of cerium chloride heptahydrate are added, and the medium is stirred for 30 minutes. 70 mg (1.9 mmol) of sodium borohydride are then added, and the reaction medium is stirred for 15 minutes until completely decolorized, and then treated with a saturated ammonium chloride solution. The residue obtained after extraction with ethyl acetate is purified by chromatography (eluent: 1 heptane/1 ethyl acetate). A white crystalline solid is obtained after recrystallization from a heptane/ethyl acetate mixture (m=180 mg; yield=42%; m.p.=175° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07468457B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-686088ddba774de086e5ca9b0baf0d00 |
| Source note | uspto-grants-2008_12 |