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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359775Generated: October 30, 2026

(4-Aminophenoxy)benzene → 6-Phenoxybenzo[d]thiazol-2-amine

https://huagongshe.com/reaction/359775

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Aminophenoxy)benzeneHCID 8764—
ReactantAmmonium thiocyanateHCID 15666—
ReactantBromineHCID 24408—
SolventAcetic AcidHCID 176—
Product6-Phenoxybenzo[d]thiazol-2-amineHCID 234499665.3%

Reaction Conditions

Temperature15 °C

Reaction Steps

20.5 g of ammonium thiocyanate were added to a solution of 25 g of 4-phenoxyaniline in 250 ml of acetic acid, and the mixture was stirred, whilst cooling. While the internal temperature was maintained at 12 to 18° C., 6.95 ml of bromine was added dropwise to the mixture. After completion of the dropwise addition, the mixture was stirred for 2 hours, after which the solvent was removed by evaporation under reduced pressure. 300ml of ethyl acetate and 200 ml of water were added to the residue, and the resulting mixture was neutralized with sodium bicarbonate. The ethyl acetate layer was separated, washed with an aqueous solution of sodium chloride, and then dehydrated over anhydrous magnesium sulfate after which it was concentrated by evaporation under reduced pressure. The solid obtained was triturated in diisopropyl ether, and filtered to give 21.34 g of the title compound, melting at 171-172° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05002942
Source datasetuspto-grants-1991_03
ORD IDord-eb29142027c147c19c01b94e4d842bec
Source noteuspto-grants-1991_03