HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → 3-Hydroxy-5-phenoxypentanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | 3-Phenoxypropanal | HCID 10986412 | — |
| Product | 3-Hydroxy-5-phenoxypentanoic acid | HCID 22024039 | — |
Reaction Steps
Magnetic microcapsules 21 were obtained in the same manner as in Example 15 except that the purified enzyme solution (1) in Example 15 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 4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07527809B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-70bad609c34645088cccda689bde1c76 |
| Source note | uspto-grants-2009_05 |