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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1806061Generated: November 2, 2026

Ammonium Chloride → 1,2-Bis(2-chloro-5-methoxyphenyl)disulfane

https://huagongshe.com/reaction/1806061

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Bromo-1-chloro-4-methoxybenzeneHCID 24212081—
ReactantSulfurothioyl dichlorideHCID 86631495—
ReactantHCID 178418918HCID 178418918—
CatalystZincchlorideHCID 3007855—
SolventTetrahydrofuranHCID 8028—
Product1,2-Bis(2-chloro-5-methoxyphenyl)disulfaneHCID 8663149421.9%

Reaction Steps

To a solution of 2-bromo-1-chloro-4-methoxybenzene (4.42 g, 19.9 mmol) in THF stirring at −10° C. under nitrogen was added isopropylmagnesium chloride (9.9 mL, 19.9 mmol, 2M in THF). The reaction was allowed to warm to ambient temperature stirred for 4 hours. The reaction was cooled to −40° C. and zinc(II) chloride (19.9 mL, 19.9 mmol, 1M in ether) was added and the solution stirred for minutes. The reaction was cooled to −78° C. and sulfurothioyl dichloride (0.80 mL, 9.9 mmol) was added. After stirring for 15 minutes at −78° C., saturated NH4Cl was added and the mixture was warmed to ambient temperature and extracted multiple times with EtOAc. The combined organic layers were dried with sodium sulfate, filtered, and concentrated to give a residue which was purified by silica chromatography (10% EtOAc in hexanes) to afford the title compound (1.52 g, 21.9% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354540B2
Source datasetuspto-grants-2013_01
ORD IDord-cf3ed80664dc44539ef081dbc3818c13
Source noteuspto-grants-2013_01