HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → Allyl 3-aminocinnamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Stannous chloride dihydrate | HCID 61436 | — |
| Reactant | HCID 54426531 | HCID 54426531 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Allyl 3-aminocinnamate | HCID 54165426 | 99.5% |
Reaction Steps
Crude allyl 3-nitrocinnamate (3 g, 12.9 mM) was dissolved in ethyl acetate (10 ml) and added slowly to a stirred suspension of SnCl2.2H2O(14.52 g, 64 mM) in ethyl acetate (20 ml). The mixture was refluxed under argon for 3 hours, cooled, and poured into a mixture of ammonia (sg 880, 15 ml) and water (5 ml). Ethyl acetate (50 ml) was added, and the organic layer separated by decantation. Two further extractions with ethyl acetate (each 50 ml) were made similarly. The combined extracts were washed with water and brine, dried (MgSO4) and evaporated to give title compound (2.6 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05527791 |
| Source dataset | uspto-grants-1996_06 |
| ORD ID | ord-2fd70fcadfa24025b57d9499fa9022d8 |
| Source note | uspto-grants-1996_06 |