HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2372549Generated: October 29, 2026
Ammonia → 2-(Diphenylphosphanyl)-6-methoxypyridine
https://huagongshe.com/reaction/2372549
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-Bromo-6-methoxypyridine | HCID 256810 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Product | 2-(Diphenylphosphanyl)-6-methoxypyridine | HCID 19802095 | — |
Reaction Steps
2.7 g Sodium was added to 100 ml liquid ammonia at -80° C., and then 15.2 g triphenylphosphine was added in 6 portions with stirring. The solution was slowly warmed to -40° C., kept at that temperature for 30 min, and then cooled again to -80° C. Then, 3.1 g ammonium chloride was added to the stirred solution, followed by 10.9 g 2-bromo-6-methoxypyridine in three portions. The cooling bath was removed and the ammonia was allowed to evaporate. The residue was worked up with water/dichloromethane as described in preparation 1. Crystallization from hexane afforded 7 g of a somewhat impure product (characterized by 31P NMR: dq =-4.4 ppm) which was used as such in the following Examples.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05099062 |
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| Source dataset | uspto-grants-1992_03 |
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| ORD ID | ord-69ec40e1b8fd49b58836a846e0093055 |
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| Source note | uspto-grants-1992_03 |
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