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1-Benzoyloxy-3-chloropropan-2-ol synthesis

9synthesis methods
-

Yield:-

Reaction Conditions:

with tetrabutylammomium bromide in ethyl acetate at 65; for 4 h;Overall yield = 87 percent; Overall yield = 3.58 g; regioselective reaction;

Steps:

Ring opening in epichlorohydrin (general procedure).

General procedure: Epichlorohydrin (21.2 mmol) and TBAB(5 mol %) were added to a solution of carboxylic acid (19.2 mmol) in EtOAc. The reaction mixture was refl uxed at 65°C for 4 h and then cooled down to room temperature and washed with a saturated Na2CO3 solution. The organic layer was dried over anhydrous Na2SO4 and evaporated to dryness, and the product was purifi ed by column chromatography on silica gel, eluentpetroleum ether-ethyl acetate, 5 : 10.

References:

Feng, Y.;He, W.;Luo, Y.;Sun, W.;Xia, X. Y.;Zhan, L. [Russian Journal of Organic Chemistry,2020,vol. 56,# 5,p. 877 - 883][Zh. Org. Khim.,2020,vol. 56,# 5,p. 877 - 883,7]