HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453095Generated: October 25, 2026
Sodium borohydride → [3-(4-Methoxyphenyl)-[1,2,4]thiadiazol-5-yl]-methanol
https://huagongshe.com/reaction/453095
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Ethyl 3-(4-methoxyphenyl)-[1,2,4]thiadiazole-5-carboxylate | HCID 12601460 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | [3-(4-Methoxyphenyl)-[1,2,4]thiadiazol-5-yl]-methanol | HCID 25132885 | 43% |
Reaction Steps
To a solution of 3-(4-methoxyphenyl)-[1,2,4]thiadiazole-5-carboxylic acid ethyl ester (0.24 g, 0.90 mmol) in MeOH (10 ml) was added sodium borohydride (0.058 g, 1.54 mmol) portion wise. The resulting reaction mixture was stirred at room temperature for 2 h. After the completion of the reaction (TLC monitoring), the reaction mass was cooled to 0° C., quenched it with 2 ml of water and concentrated under vacuum. Added water (50 ml) and extracted with ethyl acetate (3×50 ml). The combined organic layer was dried over Na2SO4, filtered and concentrated under vacuum. The crude residue was purified over silica gel (100-200 M, 20% EtOAc-Hexane) to get the product (0.072 g, 43%) that was carried forward to the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08492414B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-e2b1241a7bfc40cd8521af8989048b08 |
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| Source note | uspto-grants-2013_07 |
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