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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2280374Generated: October 30, 2026

Benzylamine → tert-Butyl 4-(benzylamino)-3,3-difluoropiperidine-1-carboxylate

https://huagongshe.com/reaction/2280374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
ReactantSodium CarbonateHCID 10340—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactanttert-Butyl 3,3-difluoro-4-oxopiperidine-1-carboxylateHCID 56776981—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 4-(benzylamino)-3,3-difluoropiperidine-1-carboxylateHCID 66710726—

Reaction Steps

To a solution of tert-butyl 3,3-difluoro-4-oxopiperidine-1-carboxylate (0.250 g, 1.06 mmol) in CH2Cl2 (4.5 mL) was added benzylamine (0.13 mL, 1.17 mmol) and sodium triacetoxyborohydride (0.356 g, 1.59 mmol) and the solution was stirred at rt for 22 h. The reaction mixture was treated with sat. aq. Na2CO3 and extracted with EA (3×50 mL). The combined organic extracts were dried over MgSO4, filtered, and the solvent removed under reduced pressure. The residue was purified by FC (Heptane/EA, 1:1) to give tert-butyl 4-(benzylamino)-3,3-difluoropiperidine-1-carboxylate. LC-MS-conditions 08: tR=0.65 min; [M+H]+=327.32.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139524B2
Source datasetuspto-grants-2015_09
ORD IDord-4499ac85e7464dd28838beef3fef46b6
Source noteuspto-grants-2015_09