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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903646Generated: October 31, 2026

Water → Benzenamine, 4-chloro-2-fluoro-5-(2-propynyloxy)-

https://huagongshe.com/reaction/1903646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Chloro-5-fluoro-4-nitro-2-(prop-2-yn-1-yloxy)benzeneHCID 13281441—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
ProductBenzenamine, 4-chloro-2-fluoro-5-(2-propynyloxy)-HCID 1327292772.6%

Reaction Conditions

Temperature90 °C

Reaction Steps

A suspension of electrolytic iron powder (3.5 g) in a 5% aqueous acetic acid solution (5 ml) was heated to 90° C., and a solution of 4-chloro-2-fluoro-5-(2-propynyloxy)nitrobenzene (5.7 g) in acetic acid (40 ml) was dropwise added thereto at the same temperature. The resultant mixture was stirred at 90°-105° C. for 1 hour and allowed to cool to room temperature. Water (200 ml) was added thereto. Insoluble materials were filtered off, and the filtrate was neutralized, followed by extraction with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and concentrated. The residue was washed with petroleum ether and carbon tetrachloride to give 3.6 g of 4-chloro-2-fluoro-5-(2-propynyloxy)aniline. M.P. 61.0°-61.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04437877
Source datasetuspto-grants-1984_03
ORD IDord-305e59a15175432da4c889242c5c8a45
Source noteuspto-grants-1984_03