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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401583Generated: October 28, 2026

Thiourea → 5-Fluoro-2-methoxyaniline

https://huagongshe.com/reaction/401583

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 numberUS08741939B2
Source datasetuspto-grants-2014_06
ORD IDord-b8678633d15540bfa250e60b49aa7c9a
Source noteuspto-grants-2014_06