HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891946Generated: October 26, 2026
Hydrochloric Acid → (5-Methoxypyridazin-3-yl)methanol
https://huagongshe.com/reaction/891946
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 23600258 | HCID 23600258 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (5-Methoxypyridazin-3-yl)methanol | HCID 22240192 | 83.4% |
Reaction Steps
5-Methoxy-pyridazine-3-carboxylic acid ethyl ester (8.1 g, 44.5 mmol) was dissolved in ethanol (105 ml) under argon. The reaction mixture was cooled to 0° C. and treated with NaBH4 (3.5 g, 89 mmol). After 10 minutes, the reaction mixture was warmed to room temperature, stirred for 1 hour and treated successively with 2N HCl and saturated sodium bicarbonate to adjust the pH at 8. The solvent was removed in vacuo and the residue was stirred with MeOH (100 ml). The suspension was filtered and the filtrate was concentrated. The residue was chromatographed over silica gel (CH2Cl2—MeOH 19:1) to provide (5-methoxy-pyridazin-3-yl)-methanol (5.2 g, 83%) as a light brown solid, MS: m/e=140 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07005432B2 |
|---|
| Source dataset | uspto-grants-2006_02 |
|---|
| ORD ID | ord-f6aeae6adc7f4e68a6cb71a2ab701636 |
|---|
| Source note | uspto-grants-2006_02 |
|---|