HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroquinone → HCID 22167616, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroquinone | HCID 785 | — |
| Reactant | Acrylic Acid | HCID 6581 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 22167614 | HCID 22167614 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 22167616 | HCID 22167616 | — |
Reaction Steps
In 270 g of 1,2-dichloroethane were added 108.11 g (1.5 mmol) of acrylic acid, 21.63 g (75 mmol) of 6-(6-hydroxy-hexa-1-yloxy)-2-naphthoic acid obtained in Step 1, 4.28 g (23 mol) of p-toluenesulfonic acid monohydrate, and 0.83 g (7.5 mmol) of hydroquinone, and the solution was refluxed for 4 hours. After evaporation of the solvent, 270 g of water was added to the residue, and the precipitate was collected by filtration and dried in an oven at 40° C. overnight. The dried product was recrystallized from acetone to yield the desired product, 6-(6-acryloyloxy-hexa-1-yloxy)-2-naphthoic acid, as light-yellow powder (16.97 g, Yield: 65%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07683203B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-c752226c42b84707b68ad5df33e9cbed |
| Source note | uspto-grants-2010_03 |