HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron trifluoride etherate → HCID 54257178, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 178476801 | HCID 178476801 | — |
| Product | HCID 54257178 | HCID 54257178 | — |
Reaction Steps
A solution of 1.68 g of ethyl 2-(4-chlorophenyl)prop-1-enylphosphinate in 20 ml of triethyl orthoformate is treated with 0.1 g of boron trifluoride diethyl etherate and the resulting solution stirred for 7 days at room temperature. The reaction mixture is then treated with 20 ml 10% aqueous sodium hydrogen carbonate solution and extracted twice with dichloromethane. The organic layer is removed, dried and concentrated to give an oil. Chromatography on silica gel gives ethyl 2-(4-chlorophenyl)prop-1-enyl-(diethoxymethyl)phosphinate as a colourless oil. 1H-NMR (CDCl3): δ(ppm)=7.38 (4H, m; Ph), 5.51 (1H, d, CH), 4.62 (1H, d, CH--P), 4.05 (2H, q, CH2OP), 3.88-3.56 (CH, m, 2×CH2OC), 2.07 (2H, d, d, CH2P), 1.28-1.14 (9H, m, 3×CH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05190934 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-553b22b701154d608d1174671f1b5804 |
| Source note | uspto-grants-1993_03 |