Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643297Generated: November 4, 2026

Acetic Acid → (S)-tert-butyl 3-(piperidin-1-ylmethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1643297

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPiperidineHCID 8082—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactanttert-Butyl (3R)-3-formylpiperidine-1-carboxylateHCID 42325667—
Product(S)-tert-butyl 3-(piperidin-1-ylmethyl)piperidine-1-carboxylateHCID 59568770—

Reaction Steps

To a solution of (R)-tert-butyl 3-formylpiperidine-1-carboxylate (110 mg, 0.51 mmol) and piperidine (53 mg, 0.62 mmol) was added NaBH(OAc)3 (153 mg, 0.73 mmol) and AcOH (37.2 mg, 35 μL, 0.62 mmol) at room temperature. The mixture was stirred for 8 h at the room temperature. The reaction was quenched by pouring into 20 mL 5% aqueous NaOH and diluted with ethylacetate. The mixture was extracted with ethyl acetate (3×15 mL) and the combined organic layers washed with brine (2×10 mL) and dried over Na2SO4. The mixture was concentrated under reduced pressure and the crude product was used directly in the next reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119692B2
Source datasetuspto-grants-2012_02
ORD IDord-53f92eb41b0c4956bad0f45be106e104
Source noteuspto-grants-2012_02