HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1942625Generated: November 3, 2026
HCID 58494117, compound → [3-(5-{3-Chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-thiadiazol-3-yl)-2-ethylphenyl]acetaldehyde
https://huagongshe.com/reaction/1942625
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 58494117 | HCID 58494117 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [3-(5-{3-Chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-thiadiazol-3-yl)-2-ethylphenyl]acetaldehyde | HCID 58494142 | 99.2% |
Reaction Steps
To a solution of 5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-3-{2-ethyl-3-[(E)-2-(methyloxy)ethenyl]phenyl}-1,2,4-thiadiazole (D51) (313 mg) in tetrahydrofuran (THF) (20 mL) stirred under nitrogen at room temperature was added 14 drops 2M hydrochloric acid. The reaction mixture was stirred at 70° C. for 4 h. After cooling the reaction, the solution was condensed under reduced pressure to give [3-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-thiadiazol-3-yl)-2-ethylphenyl]acetaldehyde (D52) (300 mg), which was used directly in the next step without further purification. MS (ES): C21H21 ClN2O2S requires 400. found 401.1 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08389508B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-8e26bfa5ea364822831f2b82755d3cb2 |
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| Source note | uspto-grants-2013_03 |
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