HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 5-Fluoronaphthalene-1-acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl (5-fluoronaphthalen-1-yl)acetate | HCID 86641635 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Fluoronaphthalene-1-acetic acid | HCID 68702393 | 82.8% |
Reaction Steps
To a solution of ethyl (5-fluoronaphthalen-1-yl)acetate (5.96 g) in ethanol (50 mL) was added 1N sodium hydroxide (50 mL), and the mixture was stirred at room temperature for 2 hr. The reaction mixture was concentrated under reduced pressure, the obtained residue was poured into water, and the mixture was washed with ethyl acetate. The aqueous layer was acidified with 1N hydrochloric acid, and extracted with chloroform, and the extract was washed with water and saturated brine, dried is over magnesium sulfate, and concentrated under reduced pressure to give (5-fluoronaphthalen-1-yl)acetic acid (4.34 g). The title compound was obtained according to the method of Example 103 and using (5-fluoronaphthalen-1-yl)acetic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08877779B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-87a05bb0138248d6b1341826929b36c7 |
| Source note | uspto-grants-2014_11 |