HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567356Generated: October 30, 2026
Sodium Hydroxide → [9-Benzyl-5-carbamoyl-1-methylcarbazol-4-yl]oxyacetic acid
https://huagongshe.com/reaction/567356
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 69867929 | HCID 69867929 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [9-Benzyl-5-carbamoyl-1-methylcarbazol-4-yl]oxyacetic acid | HCID 10271590 | 87.4% |
Reaction Steps
A slurry of 32 mg (0.0795 mmol) of [9-benzyl-5-carbamoyl-1-methylcarbazol-4-yl]oxyacetic acid methyl ester in 1 ml of tetrahydrofuran and 3.5 ml of methanol was treated with 0.3 ml of an aqueous 2 N sodium hydroxide solution and stirred overnight at room temperature. The solvent was evaporated and the residue was partitioned between 1:1 ethyl acetate/tetrahydrofuran and 0.2 N HCl solution. After another extraction with 1:1 ethyl acetate/tetrahydrofuran, the extracts were washed with brine, dried over magnesium sulfate and concentrated to afford (27 mg) of the title compound. mp. 253-254° C. ESIMS m/e 389 (M++1), 387 (M+−1) NMR (300 MHz, d6-DMSO): δ 12.83 (br, 1H); 7.75 (br, 1H); 7.53 (d, J=8.2, 1H); 7.41-7.34 (m, 2H); 7.28-7.17 (m, 3H); 7.07 (m, 2H); 6.90 (d, J=7.2, 2H); 6.49 (d, J=8.1, 1H); 5.89 (s, 2H); 4.79 (s, 2H); 2.52 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06177440B1 |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-db6fbd4acd1b413890f619bca1cd4fa5 |
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| Source note | uspto-grants-2001_01 |
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