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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490027Generated: October 31, 2026

Ethyl bromoacetate → 3-Hydroxy-5-phenoxypentanoic acid

https://huagongshe.com/reaction/490027

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
Reactant3-PhenoxypropanalHCID 10986412—
Product3-Hydroxy-5-phenoxypentanoic acidHCID 22024039—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07527809B2
Source datasetuspto-grants-2009_05
ORD IDord-7159d338d3d24a37a30f8a54ef72c09f
Source noteuspto-grants-2009_05