Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1971477Generated: November 4, 2026

Thiourea → 5-Fluoro-2-methoxyaniline

https://huagongshe.com/reaction/1971477

Reaction equation

Participants

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

Reaction Steps

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, 2H), 6.79-6.76 (m, 2H), 4.75 (br, 2H), 3.91 (s, 2H), 3.82 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431605B2
Source datasetuspto-grants-2013_04
ORD IDord-962e5827315542a1acb7df3f0de246b4
Source noteuspto-grants-2013_04