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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568514Generated: October 26, 2026

Hydroxyamine hydrochloride → (3-Bromothien-2-yl) (3-methoxyphenyl)methanone oxime

https://huagongshe.com/reaction/568514

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant(3-Bromothien-2-yl) (3-methoxyphenyl)methanoneHCID 21915416—
SolventPyridineHCID 1049—
Product(3-Bromothien-2-yl) (3-methoxyphenyl)methanone oximeHCID 7272731387%

Reaction Steps

A mixture prepared from 7 g of (3-bromothien-2-yl) (3-methoxyphenyl)methanone, 3.09 g of hydroxyamine hydrochloride and 40 ml of pyridine was stirred at room temperature overnight and thereafter heated at 100°-115° C. for 4 hours. The mixture was then quenched with water, the organics were extracted into ether, and the ether solution was washed with 3N hydrochloric acid and water and dried over anhydrous magnesium sulfate. Evaporation of the ether left a residue which crystallized upon standing overnight. The crude solid was passed through a column (alumina packed in hexane) with 15% ether/hexane used as an eluent. The solid was recrystallized from ether/hexane to give a crystalline product (6.4 g, m.p. 100°-103° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04728651
Source datasetuspto-grants-1988_03
ORD IDord-62b2f143b8034ec8b624b7d065859d69
Source noteuspto-grants-1988_03