HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30627Generated: October 27, 2026
Hydrochloric Acid → [5-(4-Fluorophenyl)-1,2,3-thiadiazol-4-yl]methanol
https://huagongshe.com/reaction/30627
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | Methyl 5-(4-fluorophenyl)-1,2,3-thiadiazole-4-carboxylate | HCID 69207857 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [5-(4-Fluorophenyl)-1,2,3-thiadiazol-4-yl]methanol | HCID 69206022 | 76.2% |
Reaction Steps
Diisobutylaluminum hydride (1.5N toluene solution, 10 ml) was added to a solution of methyl 5-(4-fluorophenyl)-1,2,3-thiadiazole-4-carboxylate (1.19 g) in tetrahydrofuran (30 ml) at 0° C. and the mixture was stirred at 0° C. for 1 hr. The reaction mixture was poured into an aqueous dilute hydrochloric acid solution and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated to give [5-(4-fluorophenyl)-1,2,3-thiadiazol-4-yl]methanol (0.80 g, yield 76%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07423159B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-c2b1b18a4158432dbb85475ba25d74f1 |
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| Source note | uspto-grants-2008_09 |
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