HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216332Generated: October 25, 2026
4-(1,2,3-Thiadiazol-4-yl)benzaldehyde → 1-[4-(1,2,3-Thiadiazol-4-yl)phenyl]ethanol
https://huagongshe.com/reaction/216332
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-(1,2,3-Thiadiazol-4-yl)benzaldehyde | HCID 2776453 | — |
| Reactant | HCID 178418332 | HCID 178418332 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-[4-(1,2,3-Thiadiazol-4-yl)phenyl]ethanol | HCID 68667674 | — |
Reaction Steps
Methylmagnesium chloride (3 M in tetrahydrofuran) (0.83 mL, 2.5 mmol) was added to a −78° C. solution of 4-(1,2,3-thiadiazol-4-yl)benzaldehyde (473 mg, 2.5 mmol) in tetrahydrofuran (10 mL). After stirring at −78° C. for 2 h, the reaction mixture was quenched with saturated aqueous ammonium chloride and extracted with ethyl acetate. The combined organic extracts were washed with brine, dried (magnesium sulfate) and concentrated in vacuo. Chromatography over silica eluting with 0-100% ethyl acetate/hexane afforded 1-[4-(1,2,3-thiadiazol-4-yl)phenyl]ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08193228B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-9a84652538d347e2ac624294d371ab00 |
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| Source note | uspto-grants-2012_06 |
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