(1S,2R,5S)-(+)-menthol is a chiral secondary alcohol. Its alcohol group can be protected as 2-tetrahydrofuranyl ether by reacting with bromotrichloromethane and tetrahydrofuran.[1]
Anwendung
(1S,2R,5S)-(+)-menthol can undergo acylation with acid anhydrides in the presence of trimethylsilyl trifluoromethanesulfonate to form the corresponding acylated products.[2]
An extremely powerful acylation reaction of alcohols with acid anhydrides catalyzed by trimethylsilyl trifluoromethanesulfonate.
Procopiou PA, et al.
The Journal of Organic Chemistry, 63(7), 2342-2347 (1998)
An efficient and extremely mild method for protecting alcohols as 2-tetrahydrofuranyl ethers.
Barks JM, et al.
Tetrahedron Letters, 41(32), 6249-6252 (2000)
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