HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2163203Generated: October 30, 2026
2-Nitroanisole → Benzenesulfonyl chloride, 4-methoxy-3-nitro-
https://huagongshe.com/reaction/2163203
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Nitroanisole | HCID 7048 | — |
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Product | Benzenesulfonyl chloride, 4-methoxy-3-nitro- | HCID 89600 | — |
Reaction Steps
2.5 mols (165 ml ) of chlorosulphonic acid are placed in a one-liter reaction vessel equipped with a stirring system, a thermometer and a dropping funnel and the acid is cooled to about 0° C with a mixture of ice and salt. 0.8 mol (100 ml) of 2-nitroanisole is added drop by drop and the solution is then allowed to come back to room temperature; after a contact time of 30 minutes, the reaction mixture is poured onto one fifth of its volume of crushed ice. The sulphonyl chloride precipitates in the form of an oil; this is extracted with chloroform. After evaporation of the organic phase, the sulphonyl chloride is crystallized in a benzene/petroleum ether mixture.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04132786 |
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| Source dataset | uspto-grants-1979_01 |
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| ORD ID | ord-804bbe9da8604ec194c3a8a52d4891dd |
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| Source note | uspto-grants-1979_01 |
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