HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-Dimethylbenzaldehyde → (3E)-4-(2,3-dimethylphenyl)but-3-enoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-Dimethylbenzaldehyde | HCID 34224 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | (2-Carboxyethyl)triphenylphosphonium bromide | HCID 2733850 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3E)-4-(2,3-dimethylphenyl)but-3-enoic acid | HCID 86728217 | 99% |
Reaction Steps
To a solution of 2,3-dimethylbenzaldehyde (17.0 g, 41.0 mmol) in THF (40 mL) was added NaHMDS (41.1 mL, 82.1 mmol) at −20° C., and the reaction was stirred for 20 min. (2-Carboxyethyl)triphenylphosphonium bromide (5.0 g, 37.3 mmol) was added to the reaction at −78° C., and reaction was stirred while warming to rt overnight. The solution was diluted with water (50 mL) and extracted with EtOAc (50×3 mL). Organics were washed with brine (50 mL), dried (Na2SO4), and concentrated to give 7.00 g (99%) of the crude title compound as a yellow solid. [M+H] calc'd for C12H14O2, 191. Found 191.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08952151B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-b0671f841761492ba4f31e06ce124fce |
| Source note | uspto-grants-2015_02 |