HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2279258Generated: October 30, 2026
Sodium borohydride → HCID 66980952, compound
https://huagongshe.com/reaction/2279258
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 67130093 | HCID 67130093 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 66980952 | HCID 66980952 | 69.5% |
Reaction Steps
To a solution of (R)-methyl 3-(4-cyano-3-(trifluoromethyl)phenyl)-1-methyl-2-oxoimidazolidine-4-carboxylate (25f) (0.330 g, 1.01 mmol) in EtOH (20 mL), cooled to 0° C., Sodium borohydride (0.045 g, 1.21 mmol) was added portion wise maintaining the temperature at 0° C. The reaction mixture was slowly warmed to room temperature and stirred for further 6 h. After completion (by TLC) the volatiles were removed under reduced pressure and the crude residue was extracted with EtOAc (3×20 mL). The combined organic extracts were dried over Na2SO4 and concentrated under reduced pressure to provide the crude reaction mixture which was purified by column chromatography to afford the alcohol 25g (0.21 g, 69%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09133182B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-89f57289508e4157a25e1c131318e192 |
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| Source note | uspto-grants-2015_09 |
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