HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715421Generated: October 29, 2026
Lithium borohydride → HCID 89874234, compound
https://huagongshe.com/reaction/715421
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | HCID 89874066 | HCID 89874066 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 89874234 | HCID 89874234 | 85.4% |
Reaction Steps
To a solution of ethyl 5-methyl-6-(2,2,2-trifluoroethoxy)pyridazine-3-carboxylate (1.70 g, 6.43 mmol, Step-2 of Amine-48) in THF (32 mL) is added a solution of lithium borohydride in THF (3 M, 3.22 mL, 9.65 mmol) at 0° C. After stirring at 0° C. for 4 hours, the reaction is quenched with saturated aqueous sodium bicarbonate solution (50 mL). The mixture is filtered through a pad of Celite, and the filtrate is extracted with EtOAc (200 mL). The separated organic layer is washed with brine, dried over sodium sulfate, and concentrated in vacuo. The residue is purified by column chromatography on silica gel eluting with n-hexane/EtOAc (1:2) to give 1.22 g (85% yield) of the title compound as white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09187475B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-e364d3ec9177481a9f196fdf7fa53186 |
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| Source note | uspto-grants-2015_11 |
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