HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 86745729, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | 1-Methyl-1-propenyl chloride | HCID 137498 | — |
| Reactant | HCID 13588529 | HCID 13588529 | — |
| Solvent | Ethanol ethylacetate | HCID 21584252 | — |
| Product | HCID 86745729 | HCID 86745729 | — |
Reaction Steps
Using the procedure for the preparation of triethyl 5-amino-1-(formylamino)-3-methylene-1,1,5-pentanetricarboxylate, chloro-methylpropene replaced the allyl bromide to obtain the expected product in the form of an oil with an Rf=0.4 in ethyl acetate/ethanol 4:1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05108990 |
| Source dataset | uspto-grants-1992_04 |
| ORD ID | ord-7501b0e8c21b4aac8cbce1dc82e5892a |
| Source note | uspto-grants-1992_04 |