Réaction #577209

ord-7159d338d3d24a37a30f8a54ef72c09f

Équation de réaction

O=CCCOc1ccccc1
3-phenoxypropanal
CCOC(=O)CBr
ethyl bromoacetate
O=C(O)CC(O)CCOc1ccccc1
3-hydroxy-5-phenoxy valeric acid

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autrewere synthesized

Mode opératoire

Magnetic microcapsules 71 were obtained in the same manner as in Example 64 except that the purified enzyme solution (1) in Example 64 was replaced by the crude enzyme solution (3) and (R)-3-hydroxybutyryl CoA was replaced by (R,S)-3-hydroxy-5-phenoxyvaleryl CoA (prepared by hydrolyzing 3-hydroxy-5-phenoxy valerate obtained through a Reformatsky reaction with zinc using 3-phenoxypropanal and ethyl bromoacetate as raw materials, which were synthesized according to a procedure described in J. Org. Chem., 55, 1490-1492, 1990, to produce 3-hydroxy-5-phenoxy valeric acid and then following a procedure described in Eur. J. Biochem., 250, 432-439, 1997). The drug content in the microcapsules is shown in Table 9.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07527809B2uspto-grants-2009_05