Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 18357471 | HCID 18357471 | — |
| Reactant | 2-fluoro-N-methoxy-N-methylbenzamide | HCID 18357556 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 18357516 | HCID 18357516 | 26.5% |
Reaction Steps
To a solution of 3 g of 3-bromo-2-(diethoxymethyl)-benzo[b]furan in 80 ml of dry ether under nitrogen at −100° C. was added 17.4 ml of a 1.7 M solution of tert-butyllithium in hexanes. The solution was stirred at the low temperature for 2 h then a solution of 2.76 g of N-methoxy-N-methyl-2-fluorobenzamide in 20 ml of dry ether was added and the solution stirred at the low tempertature for 10 min. The solution was then allowed to slowly warm to 0° C., water was added and the organic layer was separated, washed with water and dried over sodium sulfate and evaporated. Gravity chromatography eluting 0 to 50% toluene in heptane afforded 0.91 g of 2-(diethoxymethyl)-3-(2-fluorobenzoyl)-benzo[b]furan as an oil, 1H-NMR (200 MHz, CDCl3) d 5.76 (CHOEt).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06313139B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-30b6fc7969104c3a9c17a1ecf2573590 |
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| Source note | uspto-grants-2001_11 |
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