HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485962Generated: October 31, 2026
Hydrochloric Acid → HCID 178449352, compound
https://huagongshe.com/reaction/485962
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178449351 | HCID 178449351 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178449352 | HCID 178449352 | — |
Reaction Steps
2 g (5.86 millimols) of tetrachlorophthalic acid N-n-butylimide are initially introduced, together with 2.43 g (17.59 millimols) of potassium carbonate, into 15 ml of tetrahydrofuran at 0° C. A solution of 680 mg (6.16 millimols) of thiophenol in 10 ml of tetrahydrofuran is added dropwise over a period of 2 hours. The mixture is stirred at 0° C. for 3 hours and gradually warmed to 25° C. over a period of 6 hours, and then acidified with 2N HCl solution and extracted with tetrahydrofuran/toluene. After drying over sodium sulfate, the organic phase is evaporated and the residue is recrystallised several times. This yields 0.17 g (7% of theory) of 4-phenylthio-3,5,6-trichlorophthalic acid N-n-butylimide; melting point 159°-63° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04537977 |
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| Source dataset | uspto-grants-1985_08 |
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| ORD ID | ord-1647451599634c3098e911202a217ef8 |
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| Source note | uspto-grants-1985_08 |
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