HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732878Generated: October 30, 2026
N,N,N',N'-Tetramethylethylenediamine → N-Phenyl-2-(dicyclohexylphosphino)indol
https://huagongshe.com/reaction/732878
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | Chlorodicyclohexylphosphine | HCID 2734135 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | N-Phenyl-2-(dicyclohexylphosphino)indol | HCID 53411821 | — |
Reaction Steps
1.6 ml (15 mmol.) of TMEDA are added to 1.93 g (10 mmol.) of 1 in 30 ml of hexane. A solution (1.6 M in hexane) of n-BuLi (6.25 ml, 10 mmol.) is added dropwise. After 3 hours, reflux (75° C.), the colour has deepened from yellow to orange. Without cooling, a solution of 2.2 ml (10 mmol.) of chlorodicyclohexylphosphane in 20 ml of hexane is added dropwise. Refluxing is carried out for a further one hour, the colour of the mixture lightening again and a white solid precipitating. After cooling, 30 ml of water are added to the mixture. The aqueous phase is extracted 3 times using 20 ml of hexane each time. The combined organic phases are washed with 10 ml of water, dried over Na2SO4 and concentrated in vacuo (45° C.). The yellow residue is boiled for 30 minutes in 30 ml of MeOH. After cooling to RT, the resulting product is filtered off (660 mg, 17%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07589081B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-fee29dc704834d14a984a5d955705db5 |
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| Source note | uspto-grants-2009_09 |
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