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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850688Generated: October 30, 2026

Diisopropylethylamine → Tert-butyl 4-((3,3-difluoropyrrolidin-1-yl)methyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1850688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl 4-formylpiperidine-1-carboxylateHCID 1514430—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant3,3-Difluoropyrrolidine hydrochlorideHCID 24903482—
Solvent1,2-DichloroethaneHCID 11—
ProductTert-butyl 4-((3,3-difluoropyrrolidin-1-yl)methyl)piperidine-1-carboxylateHCID 86720964—

Reaction Steps

A mixture of 3,3-difluoropyrrolidine hydrochloride (965 mg, 6.722 mmol), tert-butyl 4-formylpiperidine-1-carboxylate (1.720 g, 8.066 mmol), DIPEA (955.6 mg, 1.288 mL, 7.394 mmol) and crushed 4A MS (965 mg) in DCE (30 mL) were stirred at ambient temperature for 3 hours. NaBH(OAc)3 (2.848 g, 13.44 mmol) was added and the reaction stirred at ambient temperature for a further 16 hours. The mixture was filter through Celite (washing with DCM) and the filtrate concentrated in vacuo. The residue was purified by column chromatography (ISCO Companion, 80 g column, eluting with 0 to 10% MeOH/DCM, loaded in DCM) to give the sub-title product as a colourless oil that was used directly into next step without further purification. LC-MS ES+: 305.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957078B2
Source datasetuspto-grants-2015_02
ORD IDord-3d5c529f5e3549ac98762812808967d2
Source noteuspto-grants-2015_02