HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-(2-Oxo-1,3,2-dioxaphospholan-2-yloxy)ethyl acrylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Hydroxyethyl acrylate | HCID 13165 | — |
| Reactant | 2-Chloro-1,3,2-dioxaphospholane 2-oxide | HCID 81087 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(2-Oxo-1,3,2-dioxaphospholan-2-yloxy)ethyl acrylate | HCID 13590738 | — |
Reaction Conditions
| Temperature | -20 °C |
|---|
Reaction Steps
2-Hydroxyethyl acrylate (11.5 ml, 0.1M) and triethylamine (14.6 ml) in dry diethyl ether (250 ml) were cooled to −25° C. under nitrogen as a solution of 2-chloro-2-oxo-1,3,2-dioxaphospholane (14.3 g) in dry diethyl ether was added over 20 minutes. The mixture was stirred for a further 1 hour at −20° C. and then allowed to warm to 10° C. over a further hour. The precipitate was filtered, washed with ethyl acetate (100 ml) and the combined filtrate and washings evaporated under reduced pressure to give a pale yellow oil (21 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06225431B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-f364cd0d32e44ecd80f6be24c1dfa33c |
| Source note | uspto-grants-2001_05 |