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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 925035Generated: October 27, 2026

Chlorodiphenylphosphine → HCID 178425655, compound

https://huagongshe.com/reaction/925035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorodiphenylphosphineHCID 66180—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178425630HCID 178425630—
ProductHCID 178425655HCID 178425655—

Reaction Steps

Procedure as described for NP Amidine I using the following amounts: 1.19 g of 4-methyl-N1-(2,6-dimethylphenyl)benzamidine (Amidine III, 5.0 mmol), 2.50 mL of 2.0 M butyllithium (5.0 mmol), 0.93 mL chlorodiphenylphosphine (5.0 mmol). After filtration to remove lithium chloride and removal of solvent, the oily product was treated with 20 mL of pentane. After 1 hour stiffing at room temperature, a white solid formed. The solution was concentrated to approximately 10 mL and filtered while cold, yielding 1.64 g (78%) after drying.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09283555B2
Source datasetuspto-grants-2016_03
ORD IDord-394286a4b83f40aeb9a31a1ac09c069a
Source noteuspto-grants-2016_03