HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromophenol → 3-Phenylacrylic acid 4-bromophenyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromophenol | HCID 7808 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Phenylprop-2-enoyl chloride | HCID 66023 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Phenylacrylic acid 4-bromophenyl ester | HCID 759220 | 99.8% |
Reaction Steps
An ice-cooled solution of 4-bromophenol (69.2 g) and cinnamoyl chloride (66.8 g) in dichloromethane (150 ml) was treated with triethylamine (40.6 g). After stirring for 18 hrs at room temperature the mixture was washed with water (250 ml), 1 M aqueous HCl, and dried over anhydrous sodium sulphate. Evaporation in vacuum left solid 3-phenylacrylic acid 4-bromophenyl ester (121.0 g, 99.8% yield), m.p. 113.3° C., tlc: (1) 0.83. NMR (CDCl3): 116.85, 118.87, 123.49, 128.38, 129.06, 130.90, 132.49, 134.02, 147.07, 149.84, 165.06.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07985772B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-21338b1d5d4142f9bfce44c87bb9e4c3 |
| Source note | uspto-grants-2011_07 |