HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 6-Trifluoromethoxy-2H-chromene-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 6-Trifluoromethoxy-2H-chromene-3-carbonitrile | HCID 66945244 | — |
| Product | 6-Trifluoromethoxy-2H-chromene-3-carboxylic acid | HCID 58125486 | — |
Reaction Conditions
| Temperature | 150 °C |
|---|
Reaction Steps
To a microwave vial was added 6-trifluoromethoxy-2H-chromene-3-carbonitrile (100 mg, 0.4 mmol) and 10 M of sodium hydroxide in water (2 mL, 20 mmol). The reaction mixture was heated at 150° C. for 10 minutes in the microwave. The reaction mixture was acidified with conc. HCl then extracted with EtOAc (3×30 mL). The combined organics were washed with brine (3×30 mL), dried (MgSO4), filtered and concentrated, to give the product (42 mg) as a solid. m/z=258.9 (M−1), r.t.=3.43 mins. 1H NMR (400 MHz; CDCl3) δ 7.50 (1H, s), 7.11 (1H, dd), 7.04 (1H, d), 6.84 (111, d), 5.02 (2H, d).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08163901B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-7a9b1ff7ecaa413a8b6f2954c38feb94 |
| Source note | uspto-grants-2012_04 |