HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → Methyl 3-bromocinnamate, predominantly trans
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 3-(3-Bromophenyl)-2-propen-1-ol | HCID 18676478 | — |
| Product | Methyl 3-bromocinnamate, predominantly trans | HCID 1482751 | 73% |
Reaction Steps
The title compound was prepared from trans-3-(3-bromophenyl)-2-propenol by a sequence analogous to that described above for compound (9a) but using D-(-)-diethyl tartrate. Column chromatography (ethyl acetate--light petroleum (b.p. 40-60° C.), 3:7) provided the title compound (73%) as a pale yellow oil. Distilled at 160-185° C. at 0.1 mmHg. using a Kugelrohr short path distillation apparatus as a colourless oil; [α]D25 +37.6 (c=0.020 gml-1, CHCl3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06160120 |
| Source dataset | uspto-grants-2000_12 |
| ORD ID | ord-4d9fef9211844890b29826ee635256d3 |
| Source note | uspto-grants-2000_12 |