HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 86688098, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-Bromo-5-hydroxypyridine | HCID 2762865 | — |
| Reactant | 2-Hydroxy-gamma-butyrolactone, (2R)- | HCID 7157070 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86688098 | HCID 86688098 | 79.1% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a suspension of (R)-3-hydroxydihydrofuran-2(3H)-one (500 mg, 4.9 mmol) in toluene (15 mL) was added triphenylphosphine (1.54 g, 5.88 mmol) and 6-bromopyridin-3-ol (1.02 g, 5.88 mmol). The solution was cooled to 0° C. and degassed with nitrogen bubble for 10 minutes. Di-tert-butyl diazene-1,2-dicarboxylate was dissolved in toluene (5 mL) and added over a 5 minute period. The reaction was allowed to stir for 12 hours with warming to ambient temperature. The reaction was concentrated in vacuo and the resulting material purified by silica gel chromatography eluting 1:1 hexanes/EtOAc to yield (S)-3-(6-bromopyridin-3-yloxy)dihydrofuran-2(3H)-one (1.0 g, 79%) as an off white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08754226B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-cf7dbac727cd4c9f8ea45bcd593f7c7f |
| Source note | uspto-grants-2014_06 |