HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867206Generated: November 1, 2026
Ethyl bromoacetate → 3-Hydroxy-5-phenoxypentanoic acid
https://huagongshe.com/reaction/1867206
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | 3-Phenoxypropanal | HCID 10986412 | — |
| Product | 3-Hydroxy-5-phenoxypentanoic acid | HCID 22024039 | — |
Reaction Steps
Each of the above described immobilized enzyme was suspended in 0.1 M phosphoric acid buffer (pH 7.0) 48 parts by mass. Subsequently (R,S)-3-hydroxy-5-phenoxyvaleryl CoA 1 mass part, which had been prepared by hydrolyzing 3-hydroxy-5-phenoxy valerianate obtained by Reformatsky reaction with zinc using 3-phenoxy propanal and ethyl bromoacetate that were synthesized by a method given in J. Org. Chem., 55, 1490-1492 (1990) as materials, to obtain 3-hydroxy-5-phenoxy valeric acid, and subsequently treating this was treated by a method in Eur. J. Biochem., 250, 432-439 (1997), and bovine serum albumin (manufactured by Sigma-Aldrich Com.) 0.1 mass part were added hereto. The resultant mixture was shaken gently at 30° C. for 2 hours. A blue microencapsulated pigment produced (hereinafter referred to as coloring agent) was filtrated, washed and dried, coloring agent 1 was thus obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07632618B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-d26e31af3f544379ad8f954e60542b66 |
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| Source note | uspto-grants-2009_12 |
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