HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480155Generated: October 30, 2026
Methyltriphenylphosphonium chloride → HCID 178435233, compound
https://huagongshe.com/reaction/480155
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyltriphenylphosphonium chloride | HCID 9879809 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178456486 | HCID 178456486 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178435233 | HCID 178435233 | 38% |
Reaction Steps
To a stirred suspension of methyl triphenylphosphonium chloride (1.07 g, 3.0 mmol) in THF (20 ml) at 0° C. was added n-BuLi (1.4 M in hexane, 2.14 ml, 3.0 mmol). The resulting reddish-brown mixture was stirred at this temperature for 0.5 h and then at rt for 0.5 h. A solution of 4-(2,6-dioxo-1,3-dipropyl-2,3,6,9-tetrahydro-1H-purin-8-yl)-bicyclo[2.2.2]octane-1-carbaldehyde (372 mg, 1.0 mmol) in THF (10 ml) was added over a period of 20 minutes and the resulting mixture was stirred overnight (12 h). The reaction mixture was partitioned between saturated aqeuous NH4Cl (20 ml) and EtOAc (20 ml) and the aqueous phase was extracted with EtOAc (20 ml). The combined organic extracts were washed with saturated aqeuous NaCl (50 ml), dried (MgSO4), filtered and evaporated in vacuo to afford an oil that was purified by radial chromatography (2 mm plate) using a gradient of 0-5% MeOH in CH2Cl2 as eluent. Product-containing fractions were combined and concentrated to afford 140 mg (38%) of a white solid. MS: 371 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06649600B1 |
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| Source dataset | uspto-grants-2003_11 |
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| ORD ID | ord-59076620d7f542dbacc2cc7abd315a84 |
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| Source note | uspto-grants-2003_11 |
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