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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 900642Generated: October 30, 2026

Phosphine, diethyl- → Ethanamine, 2-(diethylphosphino)-N-[2-(diethylphosphino)ethyl]-

https://huagongshe.com/reaction/900642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphine, diethyl-HCID 82948—
ReactantN,N-Bis(2-chloroethyl)-1,1,1-trimethylsilanamineHCID 323333—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178506960HCID 178506960—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductEthanamine, 2-(diethylphosphino)-N-[2-(diethylphosphino)ethyl]-HCID 437675973%

Reaction Steps

To a stirred solution of diethylphosphine (6.72 g, 74,6 mmol) in THF (150 ml) at −35° C., was added 47 ml of n-BuLi (1.6 M). Next, bis(2-chloroethyl)trimethylsilylamine (8.18 g, 38.4 mmol) in 40 ml tetrahydrofuran was then added dropwise to the LiP(Et)2 in tetrahydrofuran at −50° C. The mixture was allowed to warm to room temperature and stirred for 30 minutes. It was then heated to 60° C. and stirred overnight after which 100 ml of water was added to hydrolyse the silyl groups and the reaction mixture heated to 60° C. for 1 hour to ensure complete removal of the silyl groups. The reaction mixture was dried by passing it through a small bed of MgSO4, which was subsequently washed through with 60 ml diethyl ether. The solvent was removed to give 6.96 g bis(2-diethylphosphino-ethyl)-amine (Yield: 73%). 1H-NMR (C6D6) δ 1.12 (12H, d of t, CH2CH3, J=7.2 and 14.1 Hz), 1.38 (8H, q, CH2CH3, J=7.2), 1.60 (4H, t, (CH2)P, J=7.2) and 2.84 (4H, q, (CH2)N, J=7.8). 31P-NMR (C6D6) δ −26.02.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07361623B2
Source datasetuspto-grants-2008_04
ORD IDord-ffba5b100e734e90bfd9234306b02677
Source noteuspto-grants-2008_04