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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphine, diethyl- | HCID 82948 | — |
| Reactant | N,N-Bis(2-chloroethyl)-1,1,1-trimethylsilanamine | HCID 323333 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178506960 | HCID 178506960 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethanamine, 2-(diethylphosphino)-N-[2-(diethylphosphino)ethyl]- | HCID 4376759 | 73% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07361623B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-ffba5b100e734e90bfd9234306b02677 |
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| Source note | uspto-grants-2008_04 |
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