HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2021Generated: October 24, 2026
Ammonia → Diammonium [4-(7-ethoxymethyl-3-methylxanthin-1-yl)butyl]phosphonate
https://huagongshe.com/en/reaction/2021
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Bromotrimethylsilane | HCID 76113 | — |
| Reactant | [4-(7-Ethoxymethyl-3-methylxanthin-1-yl)butyl]phosphonate | HCID 19689210 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Diammonium [4-(7-ethoxymethyl-3-methylxanthin-1-yl)butyl]phosphonate | HCID 86752277 | — |
Reaction Steps
3.4 ml (0.026 mol) of trimethylsilyl bromide were slowly added dropwise at 0° C., under an argon atmosphere, to a solution of 4.16 g (0.01 mol) of [4-(7-ethoxymethyl-3-methylxanthin-1-yl)butyl]phosphonate in 5 ml of dichloromethane. The solution was stirred at 0° C. for 1 hour and at room temperature for 2 hours. The dichloromethane was then evaporated and the oily residue which remained was dried in a bulb tube in an oil pump vacuum to remove excess trimethylsilyl bromide and ethyl bromide formed. The residue was taken up in a little methanol and treated with 1 ml of concentrated ammonia solution and stirred at room temperature for 2 hours. After evaporating the solvent, the diammonium salt was crystallized from a methanoltdiisopropyl ether mixture.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05728686 |
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| Source dataset | uspto-grants-1998_03 |
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| ORD ID | ord-8959e916559b4ac888f77a67d88387d1 |
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| Source note | uspto-grants-1998_03 |
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