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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 901105Generated: October 31, 2026

Sodium borohydride → 1-Cyclopropylpiperidin-4-ol

https://huagongshe.com/reaction/901105

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1-Cyclopropylpiperidin-4-oneHCID 16227629—
SolventEthanolHCID 702—
Product1-Cyclopropylpiperidin-4-olHCID 5158280995%

Reaction Steps

To a cold (0° C.) solution of 1-cyclopropyl-piperidin-4-one (1.5 g, 11 mmol, 1.0 eq.) in absolute ethanol was added sodium borohydride (306 mg, 8 mmol, 0.75 eq.). The reaction mixture was stirred at room temperature for 65 h. The mixture was concentrated in vacuo. Ice water (10 mL) was added, followed by an aqueous solution of sodium hydroxide (28% w/w, ca. 10 mL) and dichloromethane (20 mL). The mixture was stirred at room temperature for 2 h. After phase separation, the aqueous layer was extracted with dichloromethane. The combined organic layers were washed with brine, dried over sodium sulfate, filtered and evaporated in vacuo. The crude mixture was purified on silica eluting with DCM/2N NH3 in methanol 93/7, yielding to 1.44 g (95%) of the desired product as a colorless oil. MS (m/e): 423.1 (MH+, 100%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07361682B2
Source datasetuspto-grants-2008_04
ORD IDord-50abefe15ada423b8b399bd0d830cded
Source noteuspto-grants-2008_04