Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylamine | HCID 1146 | — |
| Reactant | HCID 86746911 | HCID 86746911 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86746909 | HCID 86746909 | — |
Reaction Steps
A solution of 0.7 g of cholest-5-en-3β-yl (S)-2-[[(2-bromoethoxy)hydroxyphosphinyl]oxy]propionate in 15 ml of toluene is treated with 15 ml of trimethylamine in a dry-ice bath. The mixture is heated to 60° C. for 30 hours. After cooling the reaction mixture is taken up in toluene and concentrated. The residue is taken up in 30 ml of methanol, treated with 2 g of silver carbonate and stirred at 50° C. for 0.5 hour. The precipitate is filtered off, concentrated and there is obtained 0.6 g of O-[[(S)-1-[(cholest-5-en-3β-yloxy)carbonyl]ethoxy]hydroxyphosphinyl]choline hydroxide internal salt, MS: 624 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05215972 |
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| Source dataset | uspto-grants-1993_06 |
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| ORD ID | ord-2d084de03a004968b0005be89b1335a7 |
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| Source note | uspto-grants-1993_06 |
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