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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1473303Generated: November 2, 2026

Thionyl Chloride → 5-(4-Chloro-2-methoxyphenyl)naphthalene-2-sulfonyl chloride

https://huagongshe.com/reaction/1473303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium 5-(4-chloro-2-methoxyphenyl)naphthalene-2-sulfonateHCID 86687359—
Product5-(4-Chloro-2-methoxyphenyl)naphthalene-2-sulfonyl chlorideHCID 8668736189.2%

Reaction Steps

A round bottom flask was charged with sodium 5-(4-chloro-2-methoxyphenyl)naphthalene-2-sulfonate (0.137 g, 0.369 mmol) and a septum was attached and the flask flushed with N2. DMF (1.232 mL) was added followed by thionyl chloride (0.081 mL, 1.108 mmol) by syringe at rt, an exotherm was observed. The solution was maintained at rt for 1 h, and then poured into a separatory funnel containing ice. The resulting mixture was extracted with DCM (2×15 mL). The combined organic layers were washed with water (2×10 mL) and brine (1×10 mL) and dried over Na2SO4 and concentrated to give 5-(4-chloro-2-methoxyphenyl)naphthalene-2-sulfonyl chloride (0.121 g, 0.329 mmol), which was used immediately without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012443B2
Source datasetuspto-grants-2015_04
ORD IDord-ed8e263e38784056a24f2134f36fa0c4
Source noteuspto-grants-2015_04