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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51395Generated: October 29, 2026

Sodium Hydroxide → HCID 10135545, compound

https://huagongshe.com/reaction/51395

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 86756268HCID 86756268—
SolventEthanolHCID 702—
ProductHCID 10135545HCID 10135545100.7%

Reaction Steps

A suspension of the {9-[(2-cyanophenyl)methyl]-5-carbamoylcarbazol-4-yl}oxyacetic acid, methyl ester (110 mg, 0.266 mM) and 0.29 mL (0.29 mM) of 1 N NaOH in 5 mL of ethanol was sonicated for 2 hours at 25° C. The resultant white precipitate was collected by filtration, washed with small amounts of EtOH, diethyl ether, and hexanes, then dried in vacuo to afford 107 mg (95%) of the {9-[(2-cyanophenyl)methyl]-5-carbamoylcarbazol-4-yl}oxyacetic acid, sodium salt as a white powder. 1H NMR (DMSO-d6) δ7.9 (d, 1H, J=8 Hz), 7.6 (br s, 1H), 7.5 (d, 1H, J=8 Hz), 7.45-7.4 (m, 3H), 7.35 (t, 1H, J=8 Hz), 7.25 (t, 1H, J=8 Hz), 7.1 (d, 1H, J=8 Hz), 7.05 (d, 1H, J=8 Hz), 6.55 (d, 1H, J=8 Hz), 6.4 (d, 1H, J=8 Hz), 5.8 (s, 2H), and 4.3 (s, 2H). IR (KBr, cm−1) 2220, 1652, and 1613. MS (ES) m/e 398, 400.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713645B1
Source datasetuspto-grants-2004_03
ORD IDord-43ffbc79b4814ca489ee6e3141beab3f
Source noteuspto-grants-2004_03