HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030004Generated: October 27, 2026
Hydrochloric Acid → Methyl 2-(chlorosulfonyl)-6-fluorobenzoate
https://huagongshe.com/reaction/1030004
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
108 g of methyl 6-fluoroanthranilate and 45 g of sodium nitrite in 106 ml of water were added, via 2 feed devices, to 250 ml of stirred concentrated hydrochloric acid at 5° C. over the course of 1 hour in such a way that the ester component was present in excess. After the reaction mixture had been stirred for 20 minutes at 55° C.-8° C. it was poured, in one shot, into a previously prepared solution of 53 g of sulfur dioxide, 1.7 g of copper(II) chloride and a small amount of water in 200 ml of 1,2-dichloroethane, and the resulting mixture was stirred for 10 minutes thereafter. It was then slowly heated to 50° C. and stirred for 11/2 hours while introducing 46 g of sulfur dioxide. It was then cooled to 20° C. and 5.5 g of chlorine were introduced over 20 minutes, with stirring. Stirring was then continued for 20 minutes, after which the organic phase was separated off. It was washed with water, dried over magnesium sulfate and evaporated, giving 105 g of the compound shown in the title, in the form of a brownish oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05104441 |
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| Source dataset | uspto-grants-1992_04 |
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| ORD ID | ord-24aaeb07e0884701b642bdd0158e96af |
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| Source note | uspto-grants-1992_04 |
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