HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylamine → N,N-Diisopropyl-1,3,2-oxathiaphospholan-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | 2-Chloro-1,3,2-oxathiaphospholane | HCID 11194399 | — |
| Solvent | Pentane | HCID 8003 | — |
| Product | N,N-Diisopropyl-1,3,2-oxathiaphospholan-2-amine | HCID 15276683 | 70% |
Reaction Steps
Into the solution of the 2-chloro-1,3,2-oxathiaphospholane of Example 1 (28.5 g, 0.2 mol) in n-pentane (300 mL) was added dropwise, at room temperature, with stirring, N,N-diisopropylamine (40.5 g, 0.4 mol). After 0.5 h diisopropylamine hydrochloride was removed by filtration, solvent was evaporated under reduced pressure, and the product was distilled. The fraction collected at 70° C./0.1 mmHg was shown by means of 31P NMR to be homogeneous. Yield: 70%. 31P NMR: δ147.8 ppm (benzene). MS: m/z 207 (M-, E.I., 15 eV).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05512668 |
| Source dataset | uspto-grants-1996_04 |
| ORD ID | ord-e027e560682a4a66b0cb87cd02214d80 |
| Source note | uspto-grants-1996_04 |