HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356978Generated: October 30, 2026
Hydrochloric Acid → (3,5-Dichloropyridin-4-yl)methanol
https://huagongshe.com/reaction/356978
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3,5-Dichloro-4-pyridinecarboxaldehyde | HCID 2762988 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | (3,5-Dichloropyridin-4-yl)methanol | HCID 17855219 | 65.9% |
Reaction Steps
A cold (0° C.) solution of 4-formyl-3,5-dichloro-pyridine (3.0 g) in ethanol (50 mL) is treated with sodium borohydride (0.7 g), portionwise, during 5 minutes. The resulting mixture is stirred at 0° C. for 10 minutes, and then treated with aqueous hydrochloric acid (5 mL;2 M), followed by basification to pH 7 by treatment with saturated aqueous sodium hydrogen carbonate solution. The mixture is diluted with water (500 mL) and extracted with ethyl acetate (4×150 mL). The combined organic washings are dried over magnesium sulfate, and the solvent removed under reduced pressure. The resulting residue is recrystallised from t-butyl methyl ether to give 4-hydroxymethyl-3,5-dichloropyridine (2.0 g), in the form of a white solid, m.p. 87°-88° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05840724 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-cdb163daa9764927abb069a3edaaa851 |
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| Source note | uspto-grants-1998_11 |
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