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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2041996Generated: November 1, 2026

Lithium borohydride → HCID 59577304, compound

https://huagongshe.com/reaction/2041996

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium borohydrideHCID 4148881—
ReactantHCID 59577252HCID 59577252—
ProductHCID 59577304HCID 5957730424.7%

Reaction Steps

Benzyl 3-[4-(2-tert-butylphenoxy)piperidin-1-yl]-3-oxo-2-phenylpropanoate (167 mg, 0.34 mmol) obtained in Example 174 and lithium tetrahydroborate (2.0M, THF solution, 0.41 mL, 0.82 mmol) were stirred at room temperature for 3 days. The reaction mixture was partitioned between ethyl acetate and saturated aqueous ammonium chloride, and the ethyl acetate layer was dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate 75:25-25:75) to give the title compound (32 mg, 24%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586571B2
Source datasetuspto-grants-2013_11
ORD IDord-bf603a0fdd0e48d78f23abfd899e2143
Source noteuspto-grants-2013_11