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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantChlorodicyclohexylphosphineHCID 2734135—
ReactantButyllithiumHCID 178418339—
SolventHexaneHCID 8058—
ProductN-Phenyl-2-(dicyclohexylphosphino)indolHCID 53411821—

Reaction Conditions

Temperature75 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07589081B2
Source datasetuspto-grants-2009_09
ORD IDord-fee29dc704834d14a984a5d955705db5
Source noteuspto-grants-2009_09