HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669270Generated: October 30, 2026
Sodium borohydride → HCID 67342731, compound
https://huagongshe.com/reaction/1669270
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 67342066 | HCID 67342066 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67342731 | HCID 67342731 | — |
Reaction Steps
1-[2-(4-Trifluoromethyl-phenyl)-pyrimidin-5-yl]-heptan-1-one (1.47 g, 4.36 mmol) is dissolved in ethanol and cooled to 0° C. while stirring under nitrogen. To the flask is added sodium borohydride (165 mg, 4.36 mmol), and the reaction is kept at 0° C. for 1 h., then slowly warmed to room temperature. The reaction is monitored by HPLC. Upon complete consumption of starting material, the reaction is carefully quenched with water, the ethanol removed by rotary evaporator, and extracted with diethyl ether, washed, dried, and concentrated. The title compound is used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07989457B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-140af3cfd7d54359a338f149a0d8ac03 |
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| Source note | uspto-grants-2011_08 |
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