HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1849997Generated: October 25, 2026
Sodium borohydride → (5-Bromoquinolin-8-yl)methanol
https://huagongshe.com/reaction/1849997
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-Bromoquinoline-8-carboxaldehyde | HCID 16414243 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (5-Bromoquinolin-8-yl)methanol | HCID 72183353 | 100.9% |
Reaction Steps
To a solution of 5-bromoquinoline-8-carbaldehyde ([CAS 885267-41-7] 423 mg, 1.79 mmol) in MeOH (5 mL) and THF (10 mL) was added sodium borohydride (68 mg, 1.79 mmol) at 0° C. After stirring at 0° C. for 30 min, the reaction mixture was quenched with a saturated aqueous ammonium chloride solution. The mixture was extracted with ethyl acetate. The combined organic layers were washed with brine, dried with magnesium sulfate and concentrated under reduced pressure to give rise to 430 mg of the title compound as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08957051B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-e0417a9ab70e4cf1a15f473ae666edb6 |
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| Source note | uspto-grants-2015_02 |
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