HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338982Generated: October 25, 2026
Tetrahydrofuran → HCID 86707492, compound
https://huagongshe.com/reaction/338982
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | (2S)-1-methoxypropan-2-ol | HCID 6993459 | — |
| Reactant | 6-Fluoro-8-hydroxy-2-methylquinoline | HCID 66781517 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86707492 | HCID 86707492 | — |
Reaction Steps
To a solution of 6-fluoro-2-methylquinolin-8-ol (0.50 g, 2.8 mmol) in tetrahydrofuran (2.4 mL, 2.8 mmol) was added triphenylphosphine (2.6 g, 9.9 mmol), diisopropyl azodicarboxylate (0.91 mg, 4.5 mmol), and (S)-1-methoxypropan-2-ol (0.33 mg, 3.7 mmol) and the resultant mixture allowed to stir at ambient temperature for 24 hours. The reaction mixture was diluted with water (10 mL) and extracted with dichloromethane (2×20 mL). The combined organic extracts dried over sodium sulfate, filtered and concentrated under reduced pressure. Purification by normal phase chromatography on silica gel (0-2% methanol/dichloromethane) afforded the title compound which was taken on to the subsequent step without further purification, assuming theoretical yield (0.70 g, 100%) was obtained, despite being contaminated with residual triphenylphosphine oxide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08889704B2 |
|---|
| Source dataset | uspto-grants-2014_11 |
|---|
| ORD ID | ord-6be1e0c720fe4c0aac1eb0dc5a6f9ad1 |
|---|
| Source note | uspto-grants-2014_11 |
|---|