Archives for Chemistry Experiments of (S)-tert-Butyl 4-(hydroxymethyl)-2,2-dimethyloxazolidine-3-carboxylate

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Product Details of 108149-65-1, you can also check out more blogs about108149-65-1

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments. Product Details of 108149-65-1. Introducing a new discovery about 108149-65-1, Name is (S)-tert-Butyl 4-(hydroxymethyl)-2,2-dimethyloxazolidine-3-carboxylate

The title aldehyde is prepared by LiAlH4 reduction of the corresponding serine derived methyl ester to the alcohol and Swern oxidation of the latter. The aldehyde is obtained in 94 % yield and 96-98 % enantiomeric purity. This method avoids some problems encountered in the synthesis of the same aldehyde by direct controlled DIBAL reduction of the ester.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Product Details of 108149-65-1, you can also check out more blogs about108149-65-1

Reference：
Oxazolidine – Wikipedia,
Oxazolidine | C3H2298NO – PubChem