Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193479Generated: October 31, 2026

Hydrochloric Acid → HCID 21272053, compound

https://huagongshe.com/reaction/1193479

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 13515581HCID 13515581—
ReactantTin tetrachloride dihydrateHCID 85782573—
ProductHCID 21272053HCID 2127205383.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

3-Chloro-2-(2,2,2-trifluoroethoxy)nitrobenzene (47 g, 185 mmol) and tin chloride dihydrate (126.5 g, 555 mmol) were placed in a 3 neck flask equipped with an overhead stirrer. Concentrated HCl (231 mL) was added in one portion with rapid stirring, and the reaction heated rapidly until it was homogeneous. After stirring an additional 15 minutes, the mixture was cooled to 0° C. and 50% NaOH added to pH=13. The alkaline solution was extracted with Et2O (2×500 mL) and the combined Et2O layers were washed with brine (2×500 mL), dried (MgSO4), and concentrated to afford 35 g of 3-chloro-2-(2,2,2-trifluoroethoxy)aniline as a light yellow oil. This oil was dissolve in the minimum amount of ether (~100 mL), then saturated with HCl gas. The product was precipitated by the addition of hexane (250 mL), and the resulting solid removed by filtration to afford 31 g (65%) of 3-chloro-2-(2,2,2-trifluoroethoxy)aniline as the hydrochloride salt, m.p. 170°-180° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04810699
Source datasetuspto-grants-1989_03
ORD IDord-295a928d4f0343df988d66f45f949729
Source noteuspto-grants-1989_03