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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 69867929HCID 69867929—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product[9-Benzyl-5-carbamoyl-1-methylcarbazol-4-yl]oxyacetic acidHCID 1027159087.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06177440B1
Source datasetuspto-grants-2001_01
ORD IDord-db6fbd4acd1b413890f619bca1cd4fa5
Source noteuspto-grants-2001_01