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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009769Generated: October 30, 2026

Thiourea → 5-Fluoro-2-methoxyaniline

https://huagongshe.com/reaction/1009769

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioureaHCID 2723790—
Reactant5-(5-Fluoro-2-methoxybenzyl)thiazol-2-amineHCID 58032963—
Reactant2-Chloro-3-(5-fluoro-2-methoxy-phenyl)-propionaldehydeHCID 58033095—
SolventEthanolHCID 702—
Product5-Fluoro-2-methoxyanilineHCID 223105—

Reaction Steps

5-(5-Fluoro-2-methoxy-benzyl)-thiazol-2-ylamine A mixture of 2-chloro-3-(5-fluoro-2-methoxy-phenyl)-propionaldehyde (crude from above) and thiourea (29.2 g, 0.384 mol) in ethanol (400 mL) was heated to reflux for 15 hours. The solvent was removed and the residue was diluted with dichloromethane (300 mL), sodium hydroxide (10% aqueous solution, 150 mL) and water (200 mL). The aqueous phase was extracted twice with dichloromethane (150 mL). The combined organic layer was washed with water, a saturated aqueous solution of sodium chloride, dried over sodium sulfate, and evaporated to dryness. The crude product was recrystallized from a mixture of ethyl acetate and hexanes to give the pure product (6.5 g, 0.027 mol, 6.2% from 5-fluoro-2-methoxy-phenylamine). ESI-MS m/z calc. 238.1, found 239.2 (M+1)+ 1H NMR(CDCl3): δ 6.90-6.81 (m, 2 H), 6.79-6.76 (m, 2 H), 4.75 (br, 2 H), 3.91 (s, 2 H), 3.82 (s, 3 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973169B2
Source datasetuspto-grants-2011_07
ORD IDord-bbfb1bf42e6a4cf7847a34375c7075a2
Source noteuspto-grants-2011_07