HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromo-4-methoxyphenol → diethyl (2Z)-2-(2-bromo-4-methoxyphenoxy)-2-butenedioate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromo-4-methoxyphenol | HCID 297382 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | 2-Butynedioic acid, monoethyl ester | HCID 71360575 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | diethyl (2Z)-2-(2-bromo-4-methoxyphenoxy)-2-butenedioate | HCID 86587184 | 62% |
Reaction Steps
Ethyl acetylenedicarboxylate (17.8 ml, 0.145 mol) was added to 2-bromo-4-methoxyphenol (Synlett p1241, 1997) (27.3 g, 0.134 mol), in anhydrous 2-propanol (55 ml) followed by the addition of a catalytic amount of tetrabutylammonium fluoride (0.4 ml, 1.0 M in THF). The solution was stirred at room temperature overnight and was then heated to reflux for 30 min. Upon cooling a precipitate formed. The solution was cooled and filtered to give diethyl (2Z)-2-(2-bromo-4-methoxyphenoxy)-2-butenedioate as a yellow solid (29.9 g, 62% yield). Note: the solid contains 10% of diethyl (2E)-2-(2-bromo-4-methoxyphenoxy)-2-butenedioate. GC/MS (EI, M+) m/z 344 and 346.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07285662B2 |
| Source dataset | uspto-grants-2007_10 |
| ORD ID | ord-b98affa8bcd641e6ab3e3ae3054ac0a2 |
| Source note | uspto-grants-2007_10 |