HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 86746782, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Phosphoramidic acid, diphenyl ester | HCID 74836 | — |
| Reactant | 2,6-Diisopropylphenyl isocyanate | HCID 92259 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86746782 | HCID 86746782 | 66.3% |
Reaction Steps
To a suspension of diphenyl phosphoramidate (2.0 g, 8.0 mmol) in tetrahydrofuran (20 mL) at 0° C. is added 2,6-diisopropylphenyl isocyanate (1.7 mL, 8.0 mmol). Sodium hydride (0.32 g, 8.0 mmol) is then added portionwise over 15 minutes. The mixture is allowed to warm to room temperature and stirred for 6 hours. The mixture is partitioned between ethyl acetate and water and the aqueous phase is extracted three times with ethyl acetate. The combined organic extracts are washed with brine, dried over magnesium sulfate, and concentrated. Flash chromatography (7:3 hexane/ethyl acetate) affords 2.4 g of a white solid which is recrystallized (ethyl acetate/hexane) to afford 1.6 g of the title compound as a white solid; mp 171°-175° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05208224 |
| Source dataset | uspto-grants-1993_05 |
| ORD ID | ord-b3cdd4ed860d4a39acce0aa8fed602fe |
| Source note | uspto-grants-1993_05 |