HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 74016630, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 59837306 | HCID 59837306 | — |
| Reactant | HCID 131727193 | HCID 131727193 | — |
| Product | HCID 74016630 | HCID 74016630 | — |
Reaction Steps
Ethyl methylenebisphosphonate (940 mg) in THF (5 mL) was chilled to −78° C. under an argon gas atmosphere. To this solution, a 1.6 mol/L n-BuL-hexane solution (2 mL) was added dropwise and the mixture was stirred for 30 min, followed by dropwise addition of a THF solution (15 mL) of the compound of Example 193 (1.58 g). After 3 hours, a saturated ammonium chloride solution was added and the mixture was extracted with ethyl acetate. The organic phase was washed with water and a saturated aqueous solution of sodium chloride and was dried over anhydrous sodium sulfate. The solvent was removed by distillation to give the desired product as a colorless oil (1.71 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07456157B2 |
| Source dataset | uspto-grants-2008_11 |
| ORD ID | ord-3cddc6cbe8ac4e2785d7039ee39e53b5 |
| Source note | uspto-grants-2008_11 |