HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448401Generated: October 29, 2026
Hydrochloric Acid → HCID 58307330, compound
https://huagongshe.com/reaction/448401
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-Pyrrolidineethanol | HCID 76288 | — |
| Reactant | 5-Fluoro-2-nitroanisole | HCID 2779250 | — |
| Catalyst | Trioctylmethylammonium chloride | HCID 21218 | — |
| Product | HCID 58307330 | HCID 58307330 | 76% |
Reaction Steps
1-(2-Hydroxyethyl)pyrrolidine (1.6 g, 14 mmol) was added to a mixture of powdered KOH (0.78 g, 14 mmol) and Aliquat 336 (0.56 g, 1.4 mmol) and the resulting mixture was stirred for 5 minutes at 80° C. Then 4-fluoro-2-methoxy-1-nitrobenzene (2.0 g, 12 mmol) was added, and stirring proceeded at this temperature for 30 minutes. The mixture was cooled and partitioned between methylene chloride (75 mL) and water (75 mL), and the organic phase was washed with water (75 mL) and extracted with dilute aqueous HCl (3×60 mL). The combined aqueous phases were washed with methylene chloride (3×75 mL), basified (3N NaOH), and extracted with methylene chloride (3×75 mL). The combined organic extracts were washed with water (3×100 mL), dried (MgSO4), and evaporated, providing 2.4 g, in 76% yield; 1H NMR of the HCl salt (DMSO-d6) δ 1.83-2.01 (m, 4H), 3.04-3.19 (m, 4H), 3.58 (t, J=5.0 Hz, 2H), 3.94 (s, 3H), 4.51 (t, J=5.0 Hz, 2H), 6.74 (dd, J=9.0 Hz, J=2.4 Hz, 1H), 6.90 (d, J=2.4 Hz, 1H), 7.99 (d, J=9.0 Hz, 1H), 10.97 (br, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08481568B2 |
|---|
| Source dataset | uspto-grants-2013_07 |
|---|
| ORD ID | ord-70f483333a9f46419c720b75be412005 |
|---|
| Source note | uspto-grants-2013_07 |
|---|