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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1630998Generated: October 30, 2026

Sodium Hydroxide → HCID 58083444, compound

https://huagongshe.com/reaction/1630998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 58554210HCID 58554210—
SolventEthanolHCID 702—
ProductHCID 58083444HCID 58083444—

Reaction Conditions

Temperature60 °C

Reaction Steps

A 5N aqueous solution of NaOH (4.1 mL, 20.5 mmol) was added into a solution of methyl 2-ethoxy-2′-(trifluoromethyl)biphenyl-4-carboxylate (4.45 g, 13.7 mmol) in EtOH (45 mL). The reaction mixture was heated at 60° C. for 30 minutes, and then concentrated under reduced pressure. The residue was taken up with water (50 mL) and a 5N aqueous solution of HCl (7 ml), and then extracted with MTBE (2×100 mL). The organic layers were washed with brine (50 mL), dried (MgSO4) and concentrated under reduced pressure to give a colorless oil. After precipitation from pentane, the title compound was obtained as a white powder. HPLC (Method A), Rt: 4.3 min (purity: 99.7%). UPLC/MS, M−(ESI): 309.0. 1H NMR (DMSO-d6, 300 MHz) δ 13.08 (s, 1H), 7.81 (d, J=7.7 Hz, 1H), 7.70 (m, 1H), 7.64-7.54 (m, 3H), 7.33 (d, J=7.5 Hz, 1H), 7.24 (d, J=7.7 Hz, 1H), 4.04 (m, 2H), 1.12 (t, J=7.0 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791142B2
Source datasetuspto-grants-2014_07
ORD IDord-8188e018403a406492f0e344a089dceb
Source noteuspto-grants-2014_07