Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

1H-Indole-3-acetic acid, α-methyl-, methyl ester synthesis

5synthesis methods
-

Yield:23304-43-0 36%

Reaction Conditions:

Stage #1: methyl 2-(1-acetyl-1H-indol-3-yl)acetatewith lithium dipropan-2-ylazanide in tetrahydrofuran;hexane at -78; for 0.5 h;
Stage #2: iodomethane in tetrahydrofuran;hexane at -78 - 20; for 6.5 h;

References:

Fu, Beverly;Nazemi, Azadeh;Levin, Benjamin J.;Yang, Zhongyue;Kulik, Heather J.;Balskus, Emily P. [Journal of the American Chemical Society,2022,vol. 144,# 25,p. 11110 - 11119] Location in patent:supporting information