HuagongsheHuagongshe Chemistry Print Report · For research reference only
Homoallyl bromide → Diethyl 3-butenylphosphonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Homoallyl bromide | HCID 21241 | — |
| Reactant | Triethyl phosphite | HCID 31215 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Diethyl 3-butenylphosphonate | HCID 10997850 | — |
Reaction Steps
1-bromo-3-butene (39.0 mmol) and triethyl phosphite (1 g, 6 mmol) were dissolved and reacted in CHCl3 (30 mL). Then, the reaction solution was refluxed for 12 hours, cooled to room temperature and filtered through a glass filter. Chloroform (CHCl3) was completely removed from the solution under vacuum to thereby give an oily compound as the title compound. The 1H NMR results of the compound thus obtained are given as follows.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08089682B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-4a261f2dbf654a348991f1f703983f8c |
| Source note | uspto-grants-2012_01 |