HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 21403446, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Glycine, N-methyl-, ethyl ester | HCID 95849 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 21403446 | HCID 21403446 | 88.5% |
Reaction Steps
Into a 100 ml four-necked flask there were placed 11.7 g of sarcosine ethyl ester, 15 g of triethylamine and 50 ml of benzene, and 12.1 g of allyl bromide was gradually added dropwise thereto at room temperature with thorough stirring. The reaction solution was then heated and refluxed for 3 hours. After cooling, the deposited triethylamine hydrobromide was removed by filtration and the benzene removed under reduced pressure. The residue obtained was distilled under reduced pressure to obtain 13.9 g of the objective N-allylsarcosine ethyl ester (b.p.110 116° - 118° C, nD27.0 1.4308).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04054668 |
| Source dataset | uspto-grants-1977_10 |
| ORD ID | ord-ad714d55b26c479b94f4881ea6208ce5 |
| Source note | uspto-grants-1977_10 |