HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl acetate hexane → 5-Chloro-6-methoxy-3-methyl-benzofuran-2-carboxylic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | (2-Acetyl-4-chloro-5-methoxy-phenoxy)-acetic acid ethyl ester | HCID 68726576 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 5-Chloro-6-methoxy-3-methyl-benzofuran-2-carboxylic acid ethyl ester | HCID 68726997 | 40.9% |
Reaction Steps
The above prepared (2-acetyl-4-chloro-5-methoxy-phenoxy)-acetic acid ethyl ester-(6.05 g, 21.1 mmol) was dissolved in 45 mL of dimethoxyethane and treated at −15° C. with KOtBu (0.947 g, 0.4 eq.). After keeping for 45 Min. at −15° C. and 5 h at 0° C., the reaction mixture was poured onto crashed ice/HCl, twofold extracted with AcOEt, washed with water, dried over magnesium sulfate, and evaporated to dryness to leave 5.26 g of crude product. Flash chromatography (SiO2, hexane/AcOEt=9/1) of the latter afforded 2.32 g of the title compound as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07534788B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-509d6a58167443e2981b699528bb029c |
| Source note | uspto-grants-2009_05 |