HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720221Generated: October 29, 2026
Phosphate → methyl (S)-4-bromo-3-hydroxybutyrate
https://huagongshe.com/reaction/720221
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphate | HCID 1061 | — |
| Reactant | NADP nicotinamide-adenine-dinucleotide phosphate | HCID 5886 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | (2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal | HCID 107526 | — |
| Reactant | Methyl 4-bromo-3-oxobutanoate | HCID 295655 | — |
| Solvent | Butyl Acetate | HCID 31272 | — |
| Product | methyl (S)-4-bromo-3-hydroxybutyrate | HCID 11960268 | — |
Reaction Steps
Methyl 4-bromo-3-oxobutyrate (300 mg), the above-mentioned wet bacterial cells (0.4 g), NADP+ (9 mg), glucose (750 mg), glucose dehydrogenase (manufactured by Amano Pharmaceuticals, Co., Ltd.) (1.2 mg), 100 mM phosphate buffer (pH 6.5) (15 ml) and butyl acetate (15 ml) are mixed. The mixture is stirred at 30° C. for 7 hr. During the stirring, 2M aqueous sodium carbonate solution is gradually added to adjust the pH of the reaction solution to 6.5±0.2. After the stirring has been finished, the reaction solution is centrifuged (1000×g, 5 min) to collect the organic layer. The organic layer is subjected to an analysis for content using gas chromatography under the following condition. The optical purity of methyl 4-bromo-3-hydroxybutyrate in the above-mentioned organic layer was also determined under the following condition. The organic layer was concentrated to give crude methyl (S)-4-bromo-3-hydroxybutyrate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07135318B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-ff304b25119448c08723d01c7943791e |
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| Source note | uspto-grants-2006_11 |
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