HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Hydroxybenzoic Acid → 4-({6-[(3-Ethyloxetan-3-YL)methoxy]hexyl}oxy)benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Hydroxybenzoic Acid | HCID 135 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-{[(6-Bromohexyl)oxy]methyl}-3-ethyloxetane | HCID 59207310 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-({6-[(3-Ethyloxetan-3-YL)methoxy]hexyl}oxy)benzoic acid | HCID 59767596 | 66.4% |
Reaction Steps
A dimethylformamide (3 L) solution of 3-[(6-bromohexyloxy)methyl]-3-ethyloxetane 500 g, 4-hydroxybenzoic acid 297 g and potassium carbonate 490 g was stirred at 90° C. for 8 hours. Water 4 L was added to the reaction mixture, and then it was extracted with toluene 4 L. The organic layer was washed with water, and the solvent was distilled off. Sodium hydroxide 200 g, water 1 L and ethanol 2.5 L were added to the resulting residue and refluxed for 4 hours. Ethanol (1 L) was distilled off at atmospheric pressure, and then the solution was acidified by hydrochloric acid to obtain a slurry. The slurry was filtered and dried to thereby obtain 400 g of 4-[6-(3-ethyloxetane-3-ylmethoxy)hexyloxy]benzoic acid. Melting point: 58.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07381350B2 |
| Source dataset | uspto-grants-2008_06 |
| ORD ID | ord-2a05641a385e4dafafa03acb0082da18 |
| Source note | uspto-grants-2008_06 |