Reaktion #431776

ord-1003bfc266a2469b9b83c5d074b97f6e

Reaktionsgleichung

Cc1ccc([N+](=O)[O-])cc1O
2-methyl-5-nitrophenol
C=CCBr
allyl bromide
C=CCc1c(N2C(=O)C3=C(CCCC3)C2=O)ccc(Cl)c1O
3D
C=CCc1c(N2C(=O)C3=C(CCCC3)C2=O)ccc(Cl)c1O
N-(2-allyl-4-chloro-3-hydroxyphenyl)-3,4,5,6-tetrahydrophthalimide
O=[N+]([O-])c1ccc(Cl)c(O)c1
2-chloro-5-nitrophenol
C=CCBr
allyl bromide
C=CCc1c(N2C(=O)C3=C(CCCC3)C2=O)ccc(C)c1O
N-(2-allyl-3-hydroxy-4-methylphenyl)-3,4,5,6-tetrahydrophthalimide

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

N-(2-allyl-3-hydroxy-4-methylphenyl)-3,4,5,6-tetrahydrophthalimide (5A) was prepared, as yellow crystals, m.p.: 141°-143° C., from 2-methyl-5-nitrophenol and allyl bromide by the procedures described in Example 3 for preparing 3D from 2-chloro-5-nitrophenol and allyl bromide.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05053071uspto-grants-1991_10