2007
DOI: 10.14429/dsj.57.1753
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Rapid Solvent-free Synthesis of Aromatic Hydrazidesunder Microwave Irradiation

Abstract: A variety of aromatic hydrazides has been synthesised by solvent-free hydrazinolysis of corresponding esters with hydrazine hydrate under microwave irradiation.

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Cited by 13 publications
(11 citation statements)
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“…These ester yielded corresponding hydrazide on refluxing with hydrazine hydrate for 3–5 h [13]. The analytical and spectral data of hydrazides were in complete agreement with those given in literature [13–17]. Hydrazides on reaction with carbon disulphide and potassium hydroxide afforded thiocarbazate salts, which are cyclized in the presence of concentrated sulfuric acid to afford 5‐substituted‐1,3,4‐thiadiazole‐2‐thiols.…”
Section: Resultssupporting
confidence: 69%
See 1 more Smart Citation
“…These ester yielded corresponding hydrazide on refluxing with hydrazine hydrate for 3–5 h [13]. The analytical and spectral data of hydrazides were in complete agreement with those given in literature [13–17]. Hydrazides on reaction with carbon disulphide and potassium hydroxide afforded thiocarbazate salts, which are cyclized in the presence of concentrated sulfuric acid to afford 5‐substituted‐1,3,4‐thiadiazole‐2‐thiols.…”
Section: Resultssupporting
confidence: 69%
“…The product obtained was recrystallized from methyl alcohol. The hydrazides were characterized on the basis of physical and spectral data [13–17].…”
Section: Methodsmentioning
confidence: 99%
“…The product obtained was 2-hydroxybenzohydrazide (3) in 78% yield as previously reported [7]. The corresponding N'-benzylidene-2-hydroxybenzohydrazides (5a-h) obtained by condensation reaction of 2-hydroxybenzohydrazide (3) and substituted benzaldehydes (4a-h).…”
Section: Resultssupporting
confidence: 63%
“…The synthesis of 2-hydroxybenzohydra zide has been successfully done in high yield [7]. Various long chain aliphatic acid hydrazides react with by microwave irradiation technique [9].…”
Section: Introductionmentioning
confidence: 99%
“…Az irodalmi áttekintésből kitűnik, hogy a szteránváz 17-es helyzetében izoxazolokkal, A karbonsavhidrazidok egy részét (35ad) MW-besugárzás mellett metil-benzoát (34a), valamint heteroaromás észterek (34bd) és hidrazin-hidrát nukleofil acil szubsztitúciós reakciójával nyertük [153,154], majd a termékeket a feldolgozást követően tisztítás nélkül használtuk fel (32. ábra). A szteroid-karbaldehidek (32 és 33) és acil-hidrazinok (35ae) kondenzációs reakcióit hagyományos melegítés és MW-technika alkalmazásával is végrehajtottuk.…”
Section: áBra a Dea Vilsmeier-haack Reakciója éS A Főtermék Továbbalunclassified