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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058183Generated: October 31, 2026

Pyridine → HCID 12010728, compound

https://huagongshe.com/reaction/1058183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetyl chlorideHCID 6367—
ReactantAmmonium ChlorideHCID 25517—
Reactant(1R)-2'-(Diphenylphosphino)-[1,1'-binaphthalen]-2-amineHCID 10694978—
SolventDichloromethaneHCID 6344—
ProductHCID 12010728HCID 1201072888.2%

Reaction Steps

1.15 gram (2.54 mmol) of (−)-2-amino-2′-diphenylphosphino-1,1′-binaphthyl (the formula (1-1a)) was dissolved in 51 ml of methylene chloride, followed by the addition of 0.25 ml (3.04 mmol) of pyridine and 0.20 ml (2.78 mmol) of acetyl chloride under 0° C. The reaction mixture was stirred at room temperature for 3 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: 1:3 mixture of ethyl acetate and hexane) to obtain 1.11 gram of the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06515156B2
Source datasetuspto-grants-2003_02
ORD IDord-60afb80ef70d4a1f9f9281c09e1e8502
Source noteuspto-grants-2003_02