HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730033Generated: October 25, 2026
Chlorosulfonic acid → Ethyl 3-chlorosulfanyl-4-methoxybenzoate
https://huagongshe.com/reaction/730033
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Reactant | Ethyl anisate | HCID 60979 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | Ethyl 3-chlorosulfanyl-4-methoxybenzoate | HCID 86760945 | — |
Reaction Steps
A solution of ethyl 4-methoxybenzoate (15.7 g; 87.2 mmol) in CCl4 (60 ml) was cooled to −15° C., and chlorosulfonic acid (17.5 ml; 263 mmol) was added dropwise over a period of 15 min, resulting in a temperature increase to −10° C. After the addition had ended, the reaction mixture was stirred at room temperature for 2 h and then heated at 50° C. until no more starting material could be detected by thin-layer chromatography. With ice-cooling and vigorous stirring, the reaction mixture was added to a suspension of ice (50 g) in CCl4 (100 ml). The mixture was stirred vigorously for 3 min. The organic phase was separated off and the aqueous phase was extracted with CH2Cl2 (3×100 ml). The combined organic extracts were washed with saturated NaCl solution (3×), dried over Na2SO4 and concentrated. Trituration of the oily brown residue with diethyl ether resulted in 5c precipitating as a crystalline white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07582660B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-8b1f4730d34648b9b5b1ba32c747ea69 |
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| Source note | uspto-grants-2009_09 |
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