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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727385Generated: October 29, 2026

2-Bromoanisole → HCID 15871310, compound

https://huagongshe.com/reaction/727385

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromoanisoleHCID 11358—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
ReactantHCID 15871316HCID 15871316—
ReactantHCID 178489560HCID 178489560—
SolventDiethyl EtherHCID 3283—
ProductHCID 15871310HCID 1587131014%

Reaction Steps

To a solution of 2-methoxyphenylmagnesium bromide prepared from 18.7 g (0.10 mol) of 2-bromoanisole and 2.43 g (0.10 mol) of magnesium turnings in ether under dry nitrogen was added 1.6 g (5.0 mmol) of 5-amino-4-cyano-3-methylthio-1-(2,4,6-trichlorophenyl)pyrazole and the resulting mixture was stirred and refluxed for 16 hours. Upon cooling, the reaction was decomposed with 50 mL of saturated ammonium chloride solution. The organic phase was extracted with aqueous hydrogen chloride and the acidic extract was treated with 10 mL of concentrated hydrogen chloride and heated at 80°-90° C. for 10 minutes after which the mixture was cooled and made alkaline. Extraction with methylene dichloride and chromatography of the extracts with mixtures of hexane and ethyl acetate gave 313 mg (14%) of the title compound, m.p. 200°-202° C. Anal. Calcd. for C18H14O2 N3SCl3 : C, 48.82; H, 3.18; N, 9.49. Found: C, 48.54; H, 3.32; N, 9.09.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05712303
Source datasetuspto-grants-1998_01
ORD IDord-46028d3e122844049b0d9ff6790d174c
Source noteuspto-grants-1998_01