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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058182Generated: November 1, 2026

Pyridine → HCID 12010727, compound

https://huagongshe.com/reaction/1058182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethyl chloroformateHCID 6586—
ReactantAmmonium ChlorideHCID 25517—
Reactant(1R)-2'-(Diphenylphosphino)-[1,1'-binaphthalen]-2-amineHCID 10694978—
SolventDichloromethaneHCID 6344—
ProductHCID 12010727HCID 1201072792.2%

Reaction Steps

1.20 gram (2.65 mmol) of (−)-2-amino-2′-diphenylphosphino-1,1′-binaphthyl (1-1a) was dissolved in 53 ml of methylene chloride, followed by the addition of 0.26 ml (3.18 mmol) of pyridine and 0.23 ml (2.91 mmol) of methyl chloroformate under 0° C. The reaction mixture was stirred at room temperature for 21 hours. To the reaction solution, 40 ml of saturated aqueous solution of ammonium chloride was added and extracted with 100 ml of methylene chloride. The extract was washed with 80 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 1.25 gram of the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06515156B2
Source datasetuspto-grants-2003_02
ORD IDord-abcfd45c07304ea2a5acd9e0572e921b
Source noteuspto-grants-2003_02