2020
DOI: 10.1016/j.cdc.2020.100467
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Ultrasound-mediated catalyst-free protocol for the synthesis of bis-3-methyl-1-phenyl-1H-pyrazol-5-ols in aqueous ethanol

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Cited by 13 publications
(6 citation statements)
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“…The main features of the above system are green protocol, catalyst-free, rapid synthesis,simple work-up, no column chromatography and high yields (Scheme 37). [108] Hasaninejad et al developed an environment friendly and suitable approach for the synthesis of (3) by the reaction of ( 5) with ( 6) and (1) in ethanol: water system in ultrasound irradiation. This protocol offered a number of an important advantages like less reaction time, high yields and easy workup procedure (Scheme 37).…”
Section: Synthesis Of 44'-(arylmethylene)-bis-(1h-pyrazol-5-ol) Deriv...mentioning
confidence: 99%
“…The main features of the above system are green protocol, catalyst-free, rapid synthesis,simple work-up, no column chromatography and high yields (Scheme 37). [108] Hasaninejad et al developed an environment friendly and suitable approach for the synthesis of (3) by the reaction of ( 5) with ( 6) and (1) in ethanol: water system in ultrasound irradiation. This protocol offered a number of an important advantages like less reaction time, high yields and easy workup procedure (Scheme 37).…”
Section: Synthesis Of 44'-(arylmethylene)-bis-(1h-pyrazol-5-ol) Deriv...mentioning
confidence: 99%
“…Yellow solid, yield: 98%, m.p. 189–191 °C, 26 1 H NMR (400 MHz, CDCl 3 ): δ 8.19 (s, 1H, OH), 7.56–7.54 (d, J = 9.0 Hz, 5H, Ar–H), 7.23–7.21 (s, 2H, Ar–H), 7.08 (t, J = 7.8 Hz, 2H, Ar–H), 6.70–6.65 (d, J = 19.3 Hz, 4H, Ar–H), 4.68 (s, 1H, CH), 3.74 (s, 3H, OCH 3 ), 2.12 (s, 6H, 2CH 3 ). 13 C NMR (101 MHz, DMSO-d6): δ 146.79, 146.65, 146.42, 135.12, 129.49, 129.02, 126.14, 121.27, 121.20, 121.04, 120.84, 118.13, 115.30, 112.62, 112.57, 56.17, 32.81, 12.14; ESI-MS ( m / z ): 482.20 [M + ].…”
Section: Methodsmentioning
confidence: 99%
“…Light yellow crystals, yield: 95%, m.p. 194–199 °C, 26 1 H NMR (400 MHz, CDCl 3 ): δ 7.63–7.61 (d, J = 9.1 Hz, 4H, Ar–H), 7.32–7.28 (dd, J = 10.5, 4.8 Hz, 4H, Ar–H), 7.15–7.11 (m, 2H, Ar–H), 6.49 (s, 2H, Ar–H), 4.72 (s, 1H, CH), 3.77–3.3.72 (d, J = 20.3 Hz, 9H, 3OCH 3 ), 2.16 (s, 6H, 2CH 3 ). 13 C NMR (101 MHz, DMSO-d6): δ 153.06, 153.03, 153.02, 139.13, 136.38, 129.70, 129.49, 121.29, 120.90, 105.31, 60.45, 56.30, 34.33, 26.86; ESI-MS ( m / z ): 526.22 [M + ].…”
Section: Methodsmentioning
confidence: 99%
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“…Maddila et al reported an atom economical method for the synthesis of 4 H ‐chromene derivatives ( 198a‐k, 200a‐k ) using one pot multicomponent approach through ultrasound irradiation under catalyst free conditions. Method is advantageous due to 100% carbon capture and yields more than 92% (Scheme 45) [86].…”
Section: Ultrasound Synthesis Of Six Membered Heterocyclic Ringsmentioning
confidence: 99%