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ChemicalBook CAS DataBase List 2-Isopropoxyphenol
4812-20-8

2-Isopropoxyphenol synthesis

10synthesis methods
-

Yield: 88%

Reaction Conditions:

with potassium carbonate in acetone for 24 h;Reflux;Williamson synthesis;

Steps:

4.2.1. 2-Isopropoxyphenol (1a)
General procedure: A mixture of catechol (11.0 g, 100 mmol), 2-bromopropane (9.40 mL, 100 mmol), and K2CO3 (34.5 g, 250 mmol) in acetone (100 mL) was refluxed for 1 day and the reaction progress monitored by TLC. The salts were filtered off rinsing with acetone and the filtrate concentrated. The residue was partitioned between diluted aq HCl (100 mL) and Et2O (80 mL), and the product extracted with Et2O (2×80 mL). The organic layer is dried (Na2SO4) and concentrated. Kugelrohr distillation (120 °C, 10 mbar) afforded a colorless liquid (13.4 g, 88%); δH 1.35 (6H, d, J 6.1 Hz, 2Me), 4.56 (1H, sept, J 6.1 Hz, CH), 5.77 (1H, s, OH), 6.77-6.96 (4H, m). 1H NMR is in accordance with the literature data.2(b) and 17(c)

References:

Stephan, Michel;Zupancic, Borut;Mohar, Barbara [Tetrahedron,2011,vol. 67,# 34,p. 6308 - 6315] Location in patent:experimental part

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