HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 14205Generated: October 29, 2026
Potassium Hydroxide → 1-(Tert-butoxycarbonyl)-4-butyl-1,2,3,4-tetrahydroquinoxaline-6-carboxylic acid
https://huagongshe.com/reaction/14205
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 57487387 | HCID 57487387 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-(Tert-butoxycarbonyl)-4-butyl-1,2,3,4-tetrahydroquinoxaline-6-carboxylic acid | HCID 21085357 | 79.1% |
Reaction Steps
To a stirred solution of 1-tert-butyl 6-methyl 4-butyl-3,4-dihydroquinoxaline-1,6(2H)-dicarboxylate (158 mg) in methanol (1.4 mL) was added 1 M potassium hydroxide (1.4 mL). The mixture was stirred at 40° C. for 12 h and then concentrated under reduced pressure. The residue was diluted with water and washed with ethyl acetate. The aqueous layer was acidified to pH 4 with 1 N hydrochloric acid and extracted with chloroform (4×100 mL). The combined organic extracts were dried (sodium sulfate), filtered, and concentrated under reduced pressure to give 120 mg of the title compound: 1H NMR (300 MHz, CDCl3) δ 7.55, 7.40, 7.37, 3.79, 3.38, 3.34, 1.60, 1.53, 1.39, 0.97.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07727997B2 |
|---|
| Source dataset | uspto-grants-2010_06 |
|---|
| ORD ID | ord-8320fbf2dbf0480eba5cbcce559c950d |
|---|
| Source note | uspto-grants-2010_06 |
|---|