HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815493Generated: October 26, 2026
Hydrochloric Acid → (2-Isopropylphenyl)[2-nitro-4-(E-(carboxy)ethenyl)phenyl]sulfide
https://huagongshe.com/reaction/1815493
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzenethiol, 2-(1-methylethyl)- | HCID 96003 | — |
| Reactant | 3-(4-Chloro-3-nitrophenyl)acrylic acid | HCID 614919 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (2-Isopropylphenyl)[2-nitro-4-(E-(carboxy)ethenyl)phenyl]sulfide | HCID 11759679 | — |
Reaction Steps
To a stirred mixture of 4-chloro-3-nitrocinnamic acid (500 mg, 2.2 mmol) in 5 mL of anhydrous DMF with K2CO3 (911 mg, 6.6 mmol) was added 2-isopropylbenzenethiol (372 mL, 2.2 mmol) in 1 mL of DMF dropwise. The resulting mixture was then heated at 70° C. under nitrogen atmosphere overnight. Water (25 mL) was then added and the reaction mixture was acidified to pH=4 with 3N HCl. The cloudy mixture was extracted with EtOAc (2×20 mL). The combined organic layer was washed with brine, dried over Na2SO4, concentrated in vacuo to give the title compound as a viscous light-yellow oil, which was used for coupling with further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06878700B1 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-52af14d775b84026a7820109f15aaa7b |
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| Source note | uspto-grants-2005_04 |
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