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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396050Generated: November 2, 2026

2-Chloroanisole → 3-Chloro-4-methoxybenzene-1-sulfonyl chloride

https://huagongshe.com/reaction/1396050

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloroanisoleHCID 13011—
ReactantChlorosulfonic acidHCID 24638—
Product3-Chloro-4-methoxybenzene-1-sulfonyl chlorideHCID 1676742750%

Reaction Conditions

Temperature55 °C

Reaction Steps

Under N2 atmosphere, 41.25 mL chlorosulfonic acid was cooled in an ice bath, and under stirring 22.26 mL 2-chloroanisole was added dropwise. The mixture was heated to 55° C.; after 10 min. the heat source was removed and the mixture was stirred overnight at room temperature. The mixture was poured into ice water and extracted twice with DCM. The combined organic layers were dried over MgSO4 and evaporated to dryness. The residue was purified by flash chromatography (PA/EA 9:1) to give 24.94 g (50%) of a beige oil. 1H NMR (400 MHz, CDCl3) δ 4.03 (s, 3H), 7.08 (d, J=8.73 Hz, 1H), 7.94 (dd, J=9.03, 2.41 Hz, 1H), 8.06 (d, J=2.41 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901108B2
Source datasetuspto-grants-2014_12
ORD IDord-a9a85b7fd0c242e6a13eff789c5f1163
Source noteuspto-grants-2014_12