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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821622Generated: October 31, 2026

Sodium borohydride → 1-Cyclopropylpiperidin-4-ol

https://huagongshe.com/reaction/1821622

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 numberUS07608617B2
Source datasetuspto-grants-2009_10
ORD IDord-fd9c21e66fa24376a1b48f6e13252009
Source noteuspto-grants-2009_10