HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Succinate → 3-Carbomethoxy-4-(3-methoxyphenyl)-3-butenoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Succinate | HCID 7820 | — |
| Reactant | 3-Methoxybenzaldehyde | HCID 11569 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 3-Carbomethoxy-4-(3-methoxyphenyl)-3-butenoic acid | HCID 589607 | — |
Reaction Steps
To a refluxing suspension of 15.71 g (140 mmol, 1.4 eq) of potassium t-butoxide in 50 ml of t-butylalcohol is dropped in a mixture of 12.17 (100 mmol) of 3-methoxybenzaldehyde and 15.70 ml (120 mmol, 1.2 eq) of dimethyl succinate dissolved in 20 ml of t-butylalcohol. The mixture is refluxed for 3 hours, concentrated in vacuo, acidified to pH ~1 using 1N HCl, and extracted with ethylacetate. The organics are dried (MgSO4) and concentrated in vacuo to give 3-carbomethoxy-4-(3-methoxyphenyl)-3-butenoic acid in the form of a yellow oil which is used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05468898 |
| Source dataset | uspto-grants-1995_11 |
| ORD ID | ord-9dbac76f957c46e69eb4d7b1f14b508a |
| Source note | uspto-grants-1995_11 |