Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2279561Generated: October 30, 2026

Sodium Iodide → tert-Butyl 4-cyano-4-(3,4-dichlorophenyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/2279561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant15-Crown-5HCID 36336—
Reactant(3,4-Dichlorophenyl)acetonitrileHCID 76690—
ReactantN-BOC-N,N-Bis(2-chloroethyl)amineHCID 11230235—
SolventDimethylformamideHCID 6228—
Producttert-Butyl 4-cyano-4-(3,4-dichlorophenyl)piperidine-1-carboxylateHCID 4976026368%

Reaction Steps

To a stirred solution of 2-(3,4-dichlorophenyl)acetonitrile (3.50 g, 18.8 mmol, CASRN 3218-49-3) and 15-crown-5 (0.414 g, 1.88 mmol) in DMF (75 mL) at 0° C. under nitrogen was added NaH (1.88 g, 47.0 mmol, 60% mineral oil dispersion) in 2 portions. The reaction mixture was warmed to RT and stirred 35 min then re-cooled to 0° C. NaI (2.82 g, 18.8 mmol) was added followed by a solution of freshly prepared tert-butyl bis-(2-chloroethyl)carbamate (4.56 g, 18.8 mmol) in DMF (10 mL) via syringe. The reaction mixture was warmed to RT and stirred overnight. The reaction mixture was then poured into ice cold sat'd. NH4Cl solution (250 mL) with stirring and the mixture was extracted with EtOAc (2×250 mL). The combined extracts were dried (MgSO4), filtered and concentrated. The crude product was loaded onto a SiO2 column (Biotage 40L) and eluted with hexanes/EtOAc (6/1) to afford 4.54 g (68%) of tert-butyl 4-cyano-4-(3,4-dichlorophenyl)piperidine-1-carboxylate (356) as an off white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133187B2
Source datasetuspto-grants-2015_09
ORD IDord-8874d655267d4af8b81e099e585c9895
Source noteuspto-grants-2015_09