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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058184Generated: November 2, 2026

Pyridine → HCID 12010729, compound

https://huagongshe.com/reaction/1058184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzoyl chlorideHCID 7412—
ReactantAmmonium ChlorideHCID 25517—
Reactant(1R)-2'-(Diphenylphosphino)-[1,1'-binaphthalen]-2-amineHCID 10694978—
SolventDichloromethaneHCID 6344—
ProductHCID 12010729HCID 1201072994.1%

Reaction Steps

1.00 gram (2.21 mmol) of (−)-2-amino-2′-diphenylphosphino-1,1′-binaphthyl (the formula (1-1a)) was dissolved in 44 ml of methylene chloride, followed by the addition of 0.21 ml (2.65 mmol) of pyridine and 0.28 ml (2.43 mmol) of benzoyl chloride under 0° C. The reaction mixture was stirred at room temperature for 5 hours. To the reaction solution, 30 ml of saturated aqueous solution of ammonium chloride was added and extracted with 100 ml of methylene chloride. The extract was washed with 70 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: 1:6 mixture of ethyl acetate and hexane) to obtain 1.16 gram of the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06515156B2
Source datasetuspto-grants-2003_02
ORD IDord-cfdc94244a774d8bbdd5313a6be08e95
Source noteuspto-grants-2003_02