HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804063Generated: October 31, 2026
Dichloromethane → Methyl 4-bromo-2-(1,1-dioxoisothiazolidin-2-yl)benzoate
https://huagongshe.com/reaction/1804063
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Chloropropanesulphonyl chloride | HCID 15410 | — |
| Reactant | Methyl 2-Amino-4-bromobenzoate | HCID 17871390 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 4-bromo-2-(1,1-dioxoisothiazolidin-2-yl)benzoate | HCID 58484624 | — |
Reaction Steps
To a mixture of methyl 2-amino-4-bromobenzoate (5 g), triethylamine (5.73 mL), methylene chloride (39 mL) was added 3-chloropropanesulfonyl chloride (3.44 mL) under ice-cooling, and the mixture was stirred at room temperature. Water was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was washed with diluted hydrochloric acid and saturated brine, and the solvent was evaporated. To the residue were added 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) (3.9 mL) and DMF (29 mL), and the mixture was stirred at room temperature. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with diluted hydrochloric acid and saturated brine, and the solvent was evaporated. To the residue was added isopropyl ether, and the precipitated solid was collected by filtration to give the title compound (5.045 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08354401B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-d9f004fcb7054bffbb543cbfdd147709 |
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| Source note | uspto-grants-2013_01 |
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