HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-(2-Ethyl-[1,3]dioxolan-2-yl)thiophene-2-carbaldehyde → Dimethyl 4-{(e)-2-[5-(2-ethyl-[1,3]dioxolan-2-yl)-2-thienyl]vinyl}phthalate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-(2-Ethyl-[1,3]dioxolan-2-yl)thiophene-2-carbaldehyde | HCID 17934787 | — |
| Reactant | HCID 22345602 | HCID 22345602 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Dimethyl 4-{(e)-2-[5-(2-ethyl-[1,3]dioxolan-2-yl)-2-thienyl]vinyl}phthalate | HCID 20636328 | — |
Reaction Steps
18.5 g (53.7 mmol) of dimethyl 4-(diethoxyphosphorylmethyl)phthalate and 9.5 g (44.7 mmol) of 5-(2-ethyl-[1,3]dioxolan-2-yl)thiophene-2-carbaldehyde (described in Example 6(b)) are dissolved in 200 mL of anhydrous THF. 6.02 g (53.7 mmol) of potassium tert-butoxide are added and the mixture is stirred for 24 h. After the usual treatment and chromatography on silica gel (eluent: 8 heptane/2 ethyl acetate), the desired product is obtained in the form of a yellow oil (m=9.53 g, Y=53%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06706725B1 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-ce402458bdb24b5a8c0d1939ffcc1b30 |
| Source note | uspto-grants-2004_03 |