HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Ether → E-7-(4-hydroxyphenyl)hept-4-enoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Ether | HCID 8254 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | E-7-(4-Methoxyphenyl)hept-4-enoic acid | HCID 9921036 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | E-7-(4-hydroxyphenyl)hept-4-enoic acid | HCID 9899318 | — |
Reaction Steps
E-7-(4-hydroxyphenyl)hept-4-enoic acid was prepared from E-7-(4-methoxyphenyl)hept-4-enoic acid by removal of the methyl ether with boron tribromide. Boron tribromide was added to a solution of E-7-(4-methoxyphenyl)hept-4-enoic acid in methylene chloride at −78° C. and stirred for four hours. The product, E-7-(4-hydroxyphenyl)hept-4-enoic acid, was obtained by aqueous work-up of the reaction mixture followed by chromatography on silica gel, and was fully characterized by spectroscopic methods (infrared and nuclear magnetic resonance) and combustion analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06660770B2 |
| Source dataset | uspto-grants-2003_12 |
| ORD ID | ord-587ae161ca5f4f5fa49a72c8f7224750 |
| Source note | uspto-grants-2003_12 |