HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 66704611, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (-)-3-Hydroxytetrahydrofuran | HCID 641512 | — |
| Reactant | HCID 59557747 | HCID 59557747 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66704611 | HCID 66704611 | 80% |
Reaction Steps
To a stirred solution of (R)-tetrahydrofuran-3-ol (320 mg, 3.63 mmol) in dry tetrahydrofuran (10 mL) was added sodium hydride (145 mg, 3.63 mmol, 60%) slowly under 0° C. The reaction was stirred at this temperature for 30 min and then 2-(4-(5-bromo-2-chlorobenzyl)phenoxy)ethyl 4-methylbenzenesulfonate (intermediate AB) (300 mg, 0.61 mmol) was added. The reaction was warmed to room temperature and then heated to reflux overnight. The reaction was quenched with saturated ammonium chloride and extracted with ethyl acetate. The organic layer was washed with brine, dried over sodium sulfate and concentrated to a yellow oil. The crude oil was purified by flash chromatography to get 200 mg of colorless oil (80% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08106021B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-13d2b61fe8d64769908f235f01fb2284 |
| Source note | uspto-grants-2012_01 |