HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropylbenzylamine → HCID 13037511, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropylbenzylamine | HCID 66024 | — |
| Reactant | Isopropylphosphonic dichloride | HCID 2793751 | — |
| Product | HCID 13037511 | HCID 13037511 | 16% |
Reaction Steps
The procedure of Example 30 was employed utilizing N-isopropyl-N-benzylamine and isopropyl phosphonic dichloride. The reaction of the dilithio compound and the isopropyl phosphonic dichloride was conducted at -70° C. The crude product produced as a result of the chromatographic separation was distilled at 130° C. and 0.1 mm to yield a colorless oil. This oil was slurried in petroleum ether to yield 1,2-diisopropyl-2,3-dihydro-1H-2,1-benzazaphosphole-1-oxide (2.28 g, 16% yield) as a pale yellow oil having the following analysis:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04319913 |
| Source dataset | uspto-grants-1982_03 |
| ORD ID | ord-81e4f1d621bc4db7bc9cb1a61c91dd6d |
| Source note | uspto-grants-1982_03 |