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SPIRO[2.4]HEPTA-4,6-DIENE synthesis

5synthesis methods
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Yield:765-46-8 70%

Reaction Conditions:

with 2,6-di-tert-butyl-4-methyl-phenol;N-benzyl-N,N,N-triethylammonium chloride;sodium hydroxide in water at 30 - 40; for 1.5 h;

Steps:

1.2 Preparation of spiro[2.4]hepta-4,6-diene
The synthesis of spiro[2.4]hepta-4,6-diene (1) was carried out according to a modifiedmethod [2]. A mixture of freshly distilled cyclopentadiene (9.2 ml, 7.2 g, 0.11 mol), 1,2-dichloroethane (8.6 ml, 10.8 g, 0.11 mol) 2,6-di-tert-butyl-4-methylphenol (20 , 0.1 mmol)was added dropwise over 30 min to a vigorously stirred mixture of NaOH (50% aqueous solution, 24 g, 0.6 mol) and triethylbenzylammonium chloride (TEBA) (0.2 g, 1 mmol) at 30-40°C. The reaction mixture was stirred for 1 h at the same temperature. The reaction mixture wasdistilled with steam, then the organic layer was distilled under reduced pressure (60-70°/150-200 mmHg). The product yield (1) was 7.0 g (70%), purity 99% (by GLC). Physical and spectroscopic data were consistent with the literature data [2].

References:

Shulishov, Evgeny V.;Pantyukh, Olga A.;Menchikov, Leonid G.;Tomilov, Yury V. [Tetrahedron Letters,2019,vol. 60,# 31,p. 2043 - 2045] Location in patent:supporting information

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