HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716116Generated: October 30, 2026
Glyoxylic Acid → (2S,3S,4S)-4-bromo-2-fluoro-3,5-bis(benzyloxy)pentanal
https://huagongshe.com/reaction/716116
Participants
| Role | Name | HCID | Charge |
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| Reactant | Glyoxylic Acid | HCID 760 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | (2S,3S,4S)-4-bromo-2-fluoro-3,5-bis(benzyloxy)pentanal O-methyloxime | HCID 131734111 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2S,3S,4S)-4-bromo-2-fluoro-3,5-bis(benzyloxy)pentanal | HCID 118108771 | — |
Reaction Steps
3.3 mL of a 50% glyoxylic acid aqueous solution was added to a solution of 662 mg of the (2S,3S,4S)-4-bromo-2-fluoro-3,5-bis(benzyloxy)pentanal O-methyloxime in 6.6 mL of tetrahydrofuran, and the obtained mixture was then stirred at 70° C. for 4.83 hours. Thereafter, ethyl acetate and water were added to the reaction mixture. The organic layer was fractionated, and it was washed with a sodium hydrogen carbonate aqueous solution, and was then dried over anhydrous magnesium sulfate. The solvent was distilled away under reduced pressure, so as to obtain 655 mg of colorless oily (2S,3S,4S)-4-bromo-2-fluoro-3,5-bis(benzyloxy)pentanal and a water adduct thereof.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09187514B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-77bc70c6d0b245059c0a55710e1fa2c0 |
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| Source note | uspto-grants-2015_11 |
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