HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2418334Generated: November 2, 2026
Dimethylformamide → Ethyl 2-[2-nitro-3-(2-chlorophenylthio)phenyl]acetate
https://huagongshe.com/reaction/2418334
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | o-Chlorothiophenol | HCID 80599 | — |
| Reactant | Ethyl 2-(3-chloro-2-nitrophenyl)acetate | HCID 20446267 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 2-[2-nitro-3-(2-chlorophenylthio)phenyl]acetate | HCID 20446149 | — |
Reaction Steps
A mixture of 2-chlorobenzenethiol (8.0 g.), ethyl 2-(2-nitro-3-chlorophenyl)acetate (12.2 g.), anhydrous potassium carbonate (7.5 g.) and dry dimethylformamide (50 ml.) was stirred for an hour at 85° C. The reaction mixture was poured into water (300 ml.) and extracted with diethyl ether. The extract was washed with a saturated aqueous solution of sodium chloride, dried over magnesium sulfate and evaporated under reduced pressure. The oily residue was pulverized and recrystallized from methanol (20 ml.) to give the captioned compound (11.6 g.). mp 78° to 80° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04472433 |
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| Source dataset | uspto-grants-1984_09 |
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| ORD ID | ord-f6205a97ba82492d90ee4456caafdaa1 |
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| Source note | uspto-grants-1984_09 |
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