HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260581Generated: October 26, 2026
2-Methylnaphthalene → Benzyldiphenylphosphine
https://huagongshe.com/reaction/260581
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methylnaphthalene | HCID 7055 | — |
| Reactant | Chlorodiphenylphosphine | HCID 66180 | — |
| Reactant | Magnesium Chloride | HCID 5360315 | — |
| Catalyst | Benzyltrimethylammonium chloride | HCID 5963 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Benzyldiphenylphosphine | HCID 603920 | 83% |
Reaction Steps
An electrolysis cell as described in Example 1 is used. The electrolyte comprises 70 ml of dimethylformamide (max. 0.1% of water), 0.4 g of anhydrous magnesium chloride and 6.62 g (0.030 mol) of chlorodiphenylphosphine. The electrolysis is carried out as described in Example 1. The electrolysis temperature is 25° C. After an amount of charge of 0.96 Ah, the electrolysis is ended. 4.64 g (0.025 mol) of benzyltrimethylammonium chloride are then introduced into the electrolyte with exclusion of air and the mixture is stirred at 35° C. After 3 h the reaction mixture contains, according to analysis by gas chromatography (internal standard: 2-methylnaphthalene), 5.72 g of benzyldiphenylphosphine (yield 83%, based on benzyltrimethylammonium chloride used) which can be isolated by workup as described in Example 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05527967 |
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| Source dataset | uspto-grants-1996_06 |
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| ORD ID | ord-9eb794d000ea4aeabd7c743863d0fa16 |
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| Source note | uspto-grants-1996_06 |
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