Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Bromotrimethylsilane | HCID 76113 | — |
| Reactant | HCID 46865045 | HCID 46865045 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 46866644 | HCID 46866644 | 78% |
Reaction Steps
To the 1-[4-phenoxybenzenesulfonamido]-2-[diisopropylphophonoform amido]ethane (0.45 g, 0.93 mmol) in 10 ml CHCl3 was added TMSBr (5 eq, 0.62 ml, 4.6 mmol) and reaction was stirred and heated at 50° C. for 2.5 hours. The reaction mixture was monitored by 31P NMR. The solvent was evaporated and to the mixture reaction was added 5 ml MeOH for one hour. The solvent was evaporated to give a yellow oil. The product was solidified from MeCN to give 0.29 g (78%) a white solid, m.p.=166-169° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08993544B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-54ee2e31062c490bb41d5e140c03f91a |
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| Source note | uspto-grants-2015_03 |
|---|