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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430868Generated: October 30, 2026

Pyridine → HCID 12010728, compound

https://huagongshe.com/reaction/430868

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetyl chlorideHCID 6367—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 10694978HCID 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 numberUS06323353B1
Source datasetuspto-grants-2001_11
ORD IDord-43514f67ebd7400abdd47015fb40782b
Source noteuspto-grants-2001_11