Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 19020936 | HCID 19020936 | — |
| Product | HCID 20340335 | HCID 20340335 | — |
Reaction Steps
Into a round bottom flask equipped with magnetic stirrer, reflux condenser and drying tube was charged 20 ml. of dry tetrahydrofuran and 3.2 g. (0.011 moles) of 2-hydroxyethyl 2-cyano-3,3-diphenylacrylate and the solution is rapidly stirred. Then sodium hydride 0.79 g. (0.016 moles) as a 50% oil dispersion was added portionwise. To the resulting suspension was added 5.3 g. (0.044 moles) of allyl bromide and the mixture was heated at reflux (66° C.) for 5.5 hours. Upon cooling, a white insoluble solid (NaBr) was removed by filtration. The organic filtrate was evaporated, leaving as the desired product a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04202834 |
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| Source dataset | uspto-grants-1980_05 |
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| ORD ID | ord-ffadaf8e261c4bb9903b2eedb53264a1 |
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| Source note | uspto-grants-1980_05 |
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