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The starting materials were low and medium molecular weight copolymers. Infra-red spectra of
the products from the Schmidt reaction show a high degree of conversion [ 129 ]. The yields of the
oximes and subsequent Beckmann rearrangements are also high.
A Schmidt reaction on poly(
-acetyl styrene) yields a product containing acetyl amino styrene
groups in high yields and the products are surprisingly pure [ 130 ]. The solvent is acetic acid and the
converted material precipitates out as a sticky mass:
p
HN 3
H 2 SO 4
H
NH
NH 2
O
O
Another rearrangement reaction is isomerization of unsaturated polyesters upon heating. Thus, for
instance, maleate polyesters rearrange to the fumarate analogs at elevated temperatures [ 131 ]:
O
O
O
O
O
O
O
O
-stilbene moieties in the backbone can undergo
photocylization that is almost quantitative [ 473 ]:
It was reported that polymers with
cis
UV light
NBu 4 F
Δ
HCl
HO
 
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