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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587116Generated: October 29, 2026

Hexane → 1-Boc-4-Methylenepiperidine

https://huagongshe.com/reaction/587116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantPotassium tert-butoxideHCID 23665647—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventDiethyl EtherHCID 3283—
Product1-Boc-4-MethylenepiperidineHCID 275680894.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of methyltriphenylphosphonium bromide (36.3 g, 101.6 mmol, 1.35 equiv) in ether (dry, 300 mL) was added potassium t-butoxide (11 g, 98 mmol, 1.3 equiv) in one portion at 0° C. under nitrogen balloon. The mixture was then stirred at reflux for 2 hrs. The hot reaction mixture was cooled to 0° C. with an external ice-bath and then a solution of tert-butyl 4-oxopiperidine-1-carboxylate (15 g, 75.3 mmol, 1.0 equiv) in ether (60 mL) was added dropwise. The mixture was allowed to warm to room temperature and stirred at room temperature for 1 h. The mixture was then stirred at reflux overnight (16 h). The mixture was cooled to room temperature and hexane (300 mL) was added. The mixture was stirred for 10 min, filtered and eluted with Hexane/EtOAc (100/100 mL). The combined organic solution was concentrated to give the residue which was purified by CombiFlash (100 g silica gel column, EtOAc/Hex=0-30%) to afford 14 g (yield 94%) of tert-butyl 4-methylenepiperidine-1-carboxylate as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09226923B2
Source datasetuspto-grants-2016_01
ORD IDord-23e9ad5d83e14edba21f92d47c1fc3a9
Source noteuspto-grants-2016_01