HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl Alcohol → HCID 15819196, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl Alcohol | HCID 7858 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Trifluoromethylbenzylphosphonochloridic acid ethyl ester | HCID 15819195 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 15819196 | HCID 15819196 | — |
Reaction Steps
The 3-trifluoromethylbenzylphosphonochloridic acid ethyl ester of Example 4 (0.2 g, 0.7 mmol) was dissolved in 20 mL of CH2Cl2 and added slowly at 0° C. to a mixture of 1.0 mmol of allyl alcohol and 1.0 of mmol triethylamine in 20 mL of CH2Cl2. The reaction mixture was stirred for 5 hours and then diluted with H2O. The aqueous phase was further extracted 3 times with CH2Cl2. The organic extracts were combined and, after drying with anhydrous Na2SO4, were evaporated to give the crude product as an oil. Purification by column chromatography on silica gel using ethyl acetate/hexane (2.5:1) yielded 0.14 g (63%) of analytically pure product as a colorless oil. D.C.I.M.S.[MH+, 309].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05532226 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-61ab2117419b4bd7a1b24a5341c64af3 |
| Source note | uspto-grants-1996_07 |