Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058189Generated: November 2, 2026

Triethylamine → (1R)-2'-(Diphenylphosphino)-[1,1'-binaphthalen]-2-amine

https://huagongshe.com/reaction/1058189

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrichlorosilaneHCID 24811—
ReactantHCID 11465546HCID 11465546—
SolventO-XyleneHCID 7237—
Product(1R)-2'-(Diphenylphosphino)-[1,1'-binaphthalen]-2-amineHCID 1069497881.2%

Reaction Conditions

Temperature150 °C

Reaction Steps

7.16 gram (15.2 mmol) of (−)-2-amino-2′-diphenylphosphinyl-1,1′-binaphthyl (the formula (1-1a-1) was dissolved in 381 ml of xylene in an autoclave, followed by the addition of 42.5 ml (305.0 mmol) of triethylamine at 0° C. over 20 minutes and 7.70 ml (76.3 mmol) of trichlorosilane over 1 hour. The mixture was stirred at 150° C. for 18 hours in a tightly sealed condition. The reaction mixture was then extracted with 500 ml of ether. The extract was washed with 200 ml of saturated aqueous solution of ammonium chloride and 200 ml of brine, and then dried over anhydrous sodium sulfate. The solvent was evaporated under a reduced pressure. The residue was purified using a silica gel column chromatography (eluent: 1:4 mixture of ethyl acetate and hexane) to obtain 5.60 gram of the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06515156B2
Source datasetuspto-grants-2003_02
ORD IDord-a8c7d9e9fb394ed891ae16c4861706f8
Source noteuspto-grants-2003_02