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Organic Syntheses

Organic Syntheses

IF: 0.7
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Stereoretentive Iron‐catalyzed Cross‐coupling of an Enol Tosylate withMeMgBr

Published:1 January 2019 DOI: 10.1002/0471264229.OS095.27
T. Tsutsumi,?Yuichiro Ashida,?H. Nishikado,?Y. Tanabe,?Zhaobin Han,?K. Ding

Abstract

A. Methyl (Z)-2-phenyl-3-(tosyloxy)acrylate [(Z)-1)]. A 300-mL, threenecked, round-bottomed flask is attached to a CaCl2 drying tube, which is capped with a glass stopper, and fitted with a thermometer and a Tefloncoated magnetic stir bar (Note 2). Methyl 2-phenylacetate (10.54 g, 70 mmol) (Note 3), methyl formate (6.52 mL, 105 mmol) (Note 4), and THF (70 mL) (Note 5) are added and a septum is added to the middle neck. The vigorously stirred colorless solution is immersed in an ice-cooling bath, and sodium tertbutoxide (NaOt-Bu) (10.12 g, 105 mmol) (Note 6) is added in 5 portions over 5 ~ 10 min after temporarily removing the septum while maintaining the inner temperature below 10 °C (Figure 1). The suspension becomes a wellmixed pale yellow slurry (Figure 2) ca. 5 min after the addition of NaOt-Bu. A.

Substances (5)

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Sodium tert-butoxide 865-48-5 C4H9NaO 722 suppliers $11.20-$2501.30
Methyl phenylacetate 101-41-7 C9H10O2 568 suppliers $10.16-$100212.00
Methyl formate 107-31-3 C2H4O2 398 suppliers $7.62-$2347.13
Methyl (Z)-2-phenyl-3-(tosyloxy)acrylate 1188274-63-6 C17H16O5S 4 suppliers Inquiry

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