2019
DOI: 10.1002/slct.201901876
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Green Optimization of the First Steps for the Synthesis of a Novel Surfactant: Towards the Elimination of CMR Solvents and the Drastic Reduction of the Used Solvent Volume

Abstract: In this report, the first steps of the synthesis of a novel surfactant have been described. Each stage has been optimized to abide by the principles of green chemistry. The replacement of CMR (Carcinogenic, Mutagenic, Reprotoxic) solvents by 4‐MTHP (4‐methyltetrahydropyran) led to the improvement of the overall yield and to the drastic reduction of the total organic solvent volume used in the process.

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Cited by 2 publications
(2 citation statements)
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“…The proposed pathway towards molecule 1 envisioned a convergent synthetic approach involving the coupling of 8 and 10 (Figure 2). The first steps of the synthesis of 8 were performed using recently published criteria [37]. Mesylated alcohol 6 was obtained in 39% overall yield following the optimized three-step linear sequence.…”
Section: Synthesis Of the Targeted Surfactantmentioning
confidence: 99%
See 1 more Smart Citation
“…The proposed pathway towards molecule 1 envisioned a convergent synthetic approach involving the coupling of 8 and 10 (Figure 2). The first steps of the synthesis of 8 were performed using recently published criteria [37]. Mesylated alcohol 6 was obtained in 39% overall yield following the optimized three-step linear sequence.…”
Section: Synthesis Of the Targeted Surfactantmentioning
confidence: 99%
“…With respect to the imidazolidinone moiety, phenylalaninamide, which is a derivative of phenylalanine, was selected for the purposes of the present study (Figure 1). The total synthesis of this target molecule was carried out in nine steps that were optimized, fully respect the principles of green chemistry [37]. The synthesized molecule was then characterized and its surfactant aspect evaluated.…”
Section: Introductionmentioning
confidence: 99%