HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 87544705, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | p-Formylphenylboric acid | HCID 21940015 | — |
| Reactant | Methyl 3-hydroxy-5-isopropoxybenzoate | HCID 23072925 | — |
| Catalyst | Cupric acetate | HCID 8895 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 87544705 | HCID 87544705 | 57.2% |
Reaction Steps
After adding 1.05 g of molecular sieves 4 A, 1.00 g (6.70 mol) of p-formylphenylboric acid, 605 mg (3.30 mol) of copper (II) acetate and 2.32 ml (16.6 mol) of triethylamine to a solution of 700 mg (3.30 mmol) of the obtained phenol compound in methylene chloride (30 ml), the mixture was stirred at room temperature overnight under a oxygen atmosphere. The reaction mixture was filtered and then concentrated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane:acetic acid ethyl ester=5:1) to obtain 593 mg of 3-(4-formylphenoxy)-5-isopropoxybenzoic acid methyl ester (yield: 57%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07432287B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-f22f14ac63974b2ab771af105482fb90 |
| Source note | uspto-grants-2008_10 |