반응 #10703

ord-966493f923fe4472bb4fc0c0429b9e71

반응 방정식

CC(C)c1cccc(C(C)C)c1N
2,6-diisopropylaniline
c1ccncc1
pyridine
Cc1ccc(O)c(-c2c3ccccc3cc3ccccc23)c1
2-(9-Anthracenyl)-4-methylphenol
[Na+].[OH-]
NaOH
[O-]c1ccccc1
phenolate
Cc1cc(N=Nc2c(C(C)C)cccc2C(C)C)c(O)c(-c2c3ccccc3cc3ccccc23)c1
phenol
Cc1cc(N=Nc2c(C(C)C)cccc2C(C)C)c(O)c(-c2c3ccccc3cc3ccccc23)c1
2-(2′,6′-Diisopropylphenylazo)-4-methyl-6-(9-anthracenyl)phenol

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    세척In this case, the product was eluted with ether:hexanes (1:10)

실험 절차

This phenol was prepared, as described above, from a theoretical yield of 3.9 mmol of diazotized 2,6-diisopropylaniline and a phenolate solution comprised of 2-(9-Anthracenyl)-4-methylphenol (0.63 g), water (20 mL), NaOH (20 mmol), pyridine (2 mL), and benzene (4 mL). In this case, the product was eluted with ether:hexanes (1:10). Yield=0.30 g (29%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07094848B2uspto-grants-2006_08