HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64203Generated: October 30, 2026
Sodium Hydroxide → 3-Ethoxyisoquinoline-4-carboxylic acid
https://huagongshe.com/reaction/64203
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 3-ethoxyisoquinoline-4-carboxylate | HCID 90414090 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-Ethoxyisoquinoline-4-carboxylic acid | HCID 90413525 | 65.6% |
Reaction Steps
The title compound of Step B (492 mg, 2 mmol) dissolved in MeOH (15 mL) was added NaOH(aq) 2M (2.5 mL). The reaction mixture was stirred at 60° C. for 16 h and then NaOH(aq) 4M (2 mL) was added and the mixture was stirred at 70° C. for 4 h. MeOH was evaporated and the aqueous phase was cooled to 0° C. and acidified with the addition of HCl(aq) 6N. The solid was filtered, washed with cold water and dried to afford the title compound (285 mg, 65%). MS (ESI) mass calcd. for C12H11NO3, 217.1. m/z found 218.1 [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ 13.36 (s, 1H), 9.15 (s, 1H), 8.13-8.06 (m, 1H), 7.82-7.70 (m, 2H), 7.54-7.47 (m, 1H), 4.50 (q, J=7.0 Hz, 2H), 1.35 (t, J=7.0 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09447117B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-42440b634a6046d98777160111bd65db |
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| Source note | uspto-grants-2016_09 |
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