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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597791Generated: October 30, 2026

Hydrochloric Acid → 4-(5-Fluorobenzothiazol-2-ylmethoxy)aniline

https://huagongshe.com/reaction/1597791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantO-(5-Fluorobenzothiazol-2-ylmethyl)-4-nitrophenolHCID 70124450—
SolventEthanolHCID 702—
Product4-(5-Fluorobenzothiazol-2-ylmethoxy)anilineHCID 1893223773.3%

Reaction Steps

1.5 ml of concentrated hydrochloric acid were carefully added to a solution of 2.33 g of O-(5-fluorobenzothiazol-2-ylmethyl)-4-nitrophenol [prepared as described in step (a) above] in 47 ml of ethanol with stirring at room temperature and then 3.63 g of stannous chloride were added in small portions to the resulting mixture. The reaction mixture was then stirred at room temperature for 30 minutes, at the end of which time 3 ml of concentrated hydrochloric acid were added and the mixture was stirred for a further 1.5 hours at room temperature. The reaction mixture was then heated to 50° C. and stirred at this temperature for 4 hours. The reaction mixture was then cooled in an ice-water bath and 10% aqueous sodium hydroxide solution was added to said solution to adjust the pH to 10. The resulting mixture was then extracted with ethyl acetate and the resulting extract was washed consecutively with water and a saturated aqueous sodium chloride solution and then dried over anhydrous sodium sulfate. The solvent was then removed under reduced pressure and the resulting residue was recrystallized from a mixed solvent of methylene chloride and hexane to give 1.54 g (yield 73%) of the title compound as a solid having a melting point of 125° to 128° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05736487
Source datasetuspto-grants-1998_04
ORD IDord-ae71ede4b28a44e39e2d85f0d819b4ba
Source noteuspto-grants-1998_04