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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219841Generated: October 27, 2026

Hydroxylamine → Methyl 5-[amino(hydroxyimino)methyl]-2-fluorobenzoate

https://huagongshe.com/reaction/219841

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxylamineHCID 787—
ReactantWaterHCID 962—
ReactantDiethyl EtherHCID 3283—
ReactantMethyl 5-cyano-2-fluorobenzoateHCID 55265274—
SolventEthanolHCID 702—
ProductMethyl 5-[amino(hydroxyimino)methyl]-2-fluorobenzoateHCID 7230747898%

Reaction Steps

To a suspension of methyl 5-cyano-2-fluorobenzoate, obtained in step 2 (804.60 mg; 4.49 mmol; 1 eq.) in EtOH (8.05 mL) was added hydroxylamine (50% in water) (1.35 mL; 22.46 mmol; 5 eq.). The reaction mixture was stirred at RT for 1 h40. Water (25 mL) was added followed by Et2O (25 mL). Aqueous layer was extracted with Et2O (2×25 mL). The combined organic layers were then washed with NaCl sat. solution and dried over magnesium sulfate, filtered and concentrated to afford the title compound as a yellow solid (931 mg; 98%). 1H NMR (DMSO-d6, 300 MHz) δ 9.78 (br s, 1H), 8.21 (dd, J=7.1, 2.4 Hz, 1H), 7.96-7.91 (m, 1H), 7.38 (dd, J=10.8, 8.8 Hz, 1H), 5.97 (br s, 2H), 3.87 (s, 3H). HPLC (Method A), Rt 0.92 min (purity: 90.6%). LC/MS (Method B): 211.1 (M−H)−; 213.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202865B2
Source datasetuspto-grants-2012_06
ORD IDord-65828ec8a3a54301816d3ece7f6662e7
Source noteuspto-grants-2012_06