Efficient soluble polymer-supported Sharpless alkene epoxidation
catalysts
Hongchao Guo, Xueyan Shi, Zhen Qiao, Shicong Hou and Min Wang*
College of Applied Chemistry, China Agricultural University, Beijing 100094, China.
E-mail: wangmin@mail.cau.edu.cn
Received (in Cambridge, UK) 30th August 2001, Accepted 25th October 2001
First published as an Advance Article on the web 7th January 2002
High chemical yields and good enantiomeric excesses are
obtained by using soluble polymer-supported tartrate ester
in the epoxidation of trans-hex-2-en-1-ol using Ti(OPri)4/
tert-butyl hydroperoxide.
Since the initial solid-phase synthesis of oligopeptides was
introduced by Merrifield,1 the use of insoluble polymers as
supports for reagents and catalysts for various reactions has
increased and achieved wide recognition.2–7 Although insoluble
polymer-supported reactive species have many advantages,
there are limitations associated with these species.8 Soluble
Scheme 2 Reagents and conditions: MeOPEGOHNMeO–(CH2CH2O)n–
CH2CH2OH; i, p-toluenesulfonic acid (5 mass%), ca. 115 °C, 45 h; ii,
CH2N2, rt.
polymer-bound ligands, reagents, or catalysts as an alternative
to insoluble polymer-bound reagents or catalysts have under-
gone considerable progress in recent years.9–11 Synthetic
approaches utilizing soluble polymers couple the advantages of
homogeneous solution chemistry such as high reactivity, lack of
diffusion phenomena and ease of analysis with the advantages
of solid phase methods, such as use of excess of reagents, easy
isolation and purification of products.
Scheme 3 Reagents and conditions: i, tartrate ester (6–48 mol%), Ti(OPri)4
(5–20 mol%), ButOOH (2 equiv.), 4 Å sieves, CH2Cl2, 220 °C to 215 °C,
However, there are few reports of the immobilization of the
Sharpless Ti–tartrate ester-based asymmetric alkene epoxida-
tion catalyst using souble-polymers. The linear poly(tartrate
ester) system developed by Sherrington and coworkers was
successful,12 the observed enantioselectivity for epoxidation
was up to 79% ee (enantiomer excess). However compared with
5 h.
additional 5 h at 220 to 215 °C, then the GC yield was
determined. The mixture was treated according to workup A15
with some modification. The CH2Cl2 was removed by distilla-
tion under reduced pressure at 25 °C, then diethyl ether added to
the resulting mixture to precipitate the tartrate under vigorous
stirring conditions, and filtered to obtain the slightly yellow
tartrate ligand, with a recovery level of > 98%. The filtrate was
treated with ferrous sulfate and tartaric acid as described in
workup A.15 Product 7 was isolated via Kugelrohr distillation,
and after 7 was derivatized as its acetate, the ee was determined
with a chiral capillary gas chromatography column the chiral
stationary phase of which was 2,6-di-O-benzyl-3-O-heptano-
ylcyclodextrin. Each peak was identified by GC/MS. Results
are summarized in Table 1. The enantioselectivities varied
significantly with different ligand : Ti ratios. With 3a, 3b and 5,
up to 93, 93 and 90% ee were obtained, respectively. Generally,
isolated yields were low because of the small scale of the
reactions, and neither GC yields nor isolated yields were
optimized. There should, however, be considerable scope for
optimization. Surprisingly, (2)-(2S,3S)-trans-7 was obtained
using 3a, yet (+)-(2R,3R)-trans-7 was obtained using 3b or 5.
This was established by measuring the optical rotation and also
by GC analyses. After the sample of 7 prepared using 3a and
another sample prepared using 3b or 5 was mixed, the ee of the
resulting mixture was lower than the ee of each single sample.
The different absolute configuration of 7 resulting from
different ligands may involve a contribution from molecular
weight variation and conformational factors, but the influence
of the linear polymer chain is not clear.
the 98% ee obtained by the solution-phase reaction with -
L
(+)-dimethyl tartrate, the enantioselectivity was moderate and
the catalytic system requires improving. We now report the
synthesis of a group of tartrate esters and their use with titanium
tetraisopropoxide [Ti(OPri)4] and tert-butyl hydroperoxide
(tBHP) as the oxidant in epoxidising trans-hex-2-en-1-ol in
high chemical yield and good ee.
Tartrate esters 3a and 3b were synthesized from -(+)-tartaric
L
acid and polyethylene glycol monomethyl ether as described by
Yamamoto and coworkers13 (Scheme 1). After reaction, the
solvent toluene was removed by distillation under reduced
pressure at the end of the reaction and the resulting solid was
then dissolved using a small amount of CH2Cl2. Diethyl ether
was added to the resulting solution to precipitate the tartrate
ester under ice-salt cooling, and tartrate esters were obtained by
filtration. Tartrate 5 was synthesized from -(+)-tartaric acid by
L
two steps (Scheme 2). Tartrates 3a, 3b and 5 were identified by
1H NMR and IR.14
Tartrates 3a, 3b and 5 were used as ligands in the epoxidation
of 6 with Ti(OPri)4/tBHP as shown in Scheme 3. Powdered
activated 4 Å molecular sieves, tartrate ligand and Ti(OPri)4
were first mixed in CH2Cl2 at 220 °C, then tBHP in isooctane
was added and the mixture stirred for 1 h at 220 °C before 6 in
CH2Cl2 was added. The resulting mixture was stirred for an
1H NMR spectroscopic analysis showed the recovered
tartrate to have the same characteristic peaks as before the
reaction, indicating that in principle the soluble polymer-ligand
might be reused. The ligand 3b was recycled four times, but
only moderate ee values were obtained. The ee from the first to
fourth recycle were 49, 44, 32 and 30%, respectively. Although
the recycle results were not satisfactory, the recovery of ligand
Scheme 1 Reagents and conditions: MeOPEGOHNMeO–(CH2CH2O)n–
CH2CH2OH; i, p-toluenesulfonic acid (5 mass%), ca. 115 °C, 45 h.
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CHEM. COMMUN., 2002, 118–119
This journal is © The Royal Society of Chemistry 2002