HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Butenenitrile, 2-(acetyloxy)- → n-Pentyl (3-acetoxy-3-cyanopropyl)methylphosphinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Butenenitrile, 2-(acetyloxy)- | HCID 85891 | — |
| Reactant | n-Pentyl methanephosphonite | HCID 131714778 | — |
| Product | n-Pentyl (3-acetoxy-3-cyanopropyl)methylphosphinate | HCID 53637752 | 101.1% |
Reaction Steps
242.0 g of n-pentyl methanephosphonite are heated to 80° C. under nitrogen, and 0.5 g of tert.-butyl perpivalate is added. 63.9 g of acrolein cyanohydrin acetate mixed with 2.5 g of tert.-butyl perpivalate are added dropwise to this solution within 2.25 hours. After reaction is complete, the mixture is stirred for 5 minutes, and 161.5 g of n-pentyl methanephosphonite are distilled out. (Purity: 91.2%, recovery: 93.4%). 142.1 g of n-pentyl (3-acetoxy-3-cyanopropyl)methylphosphinate (purity 94%; yield 97%) remain.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04599207 |
| Source dataset | uspto-grants-1986_07 |
| ORD ID | ord-4b550c9c938748bd86726c3ab044f4d6 |
| Source note | uspto-grants-1986_07 |