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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 925055Generated: October 30, 2026

Chlorodiphenylphosphine → HCID 178420371, compound

https://huagongshe.com/reaction/925055

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorodiphenylphosphineHCID 66180—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178512080HCID 178512080—
SolventPentaneHCID 8003—
ProductHCID 178420371HCID 17842037126.8%

Reaction Steps

Procedure as described for NP Amidine XVII using the following amounts: 3.06 g of N1-(thiazol-2-yl)benzamidine (Amidine XVI, 15.0 mmol), 7.50 mL of 2.0 M butyllithium (15.0 mmol), 0.93 mL of chlorodiphenylphosphine (15.0 mmol). Following removal of lithium chloride, the solvent was removed from the filtrate to give a sticky residue. The sticky residue was suspended in 100 mL of pentane. Vigorous stirring and scraping eventually yielded an off-white solid after 2 hours. The solid was collected and dried (2.59 g). The lithium chloride solid separated from reaction solution was extracted with 100 mL of diethylether, filtered, taken to dryness, and treated with 100 mL of pentane. Stirring and scraping produced white solid that was collected and dried yielding an additional 1.56 g of solid. Combined yield 4.15 g (71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09283555B2
Source datasetuspto-grants-2016_03
ORD IDord-d3f6520c8e5345d2aa59e0ad19173175
Source noteuspto-grants-2016_03