HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 925055Generated: October 30, 2026
Chlorodiphenylphosphine → HCID 178420371, compound
https://huagongshe.com/reaction/925055
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorodiphenylphosphine | HCID 66180 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178512080 | HCID 178512080 | — |
| Solvent | Pentane | HCID 8003 | — |
| Product | HCID 178420371 | HCID 178420371 | 26.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09283555B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-d3f6520c8e5345d2aa59e0ad19173175 |
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| Source note | uspto-grants-2016_03 |
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