HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2372645Generated: October 30, 2026
Hydrochloric Acid → Methyl 2-(chlorosulfonyl)-6-fluorobenzoate
https://huagongshe.com/reaction/2372645
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sulfur Dioxide | HCID 1119 | — |
| Reactant | Chlorine | HCID 24526 | — |
| Reactant | Methyl 2-amino-6-fluorobenzoate | HCID 2818492 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Catalyst | Cupric Chloride | HCID 24014 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 2-(chlorosulfonyl)-6-fluorobenzoate | HCID 14257491 | — |
Reaction Steps
At 5° C. and while stirring, 108 g (0.64 mol) of methyl 6-fluoroanthranilate and 45 g (0.65 mol) of sodium nitrite in 106 ml of water were added separately but simultaneously over a period of 1 hour in such a manner to 250 ml of concentrated hydrochloric acid that the ester component was in an excess. After the reaction mixture had been stirred for 20 minutes at 5° to 8° C., it was poured all at once into a prepared solution of 53 g of sulfur dioxide, 1.7 g of copper(II) chloride in a small amount of water and 200 ml of 1,2-dichloroethane, and stirred for a further 10 minutes. The mixture was heated slowly to 50° C. and stirred for ninety minutes while passing in 46 g of sulfur dioxide. The mixture was then cooled to 20° C. and 5.5 g of chlorine was passed in over a 20-minute period while stirring. The organic phase was then separated, washed with water and dried. There was obtained 65% of theory of the title compound as a brownish oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05100459 |
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| Source dataset | uspto-grants-1992_03 |
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| ORD ID | ord-d1dc040744334c89b88cd9312c40e859 |
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| Source note | uspto-grants-1992_03 |
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