HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1513372Generated: November 3, 2026
L-Tartaric acid → 2,3-Dihydroxybutanedioic Acid
https://huagongshe.com/reaction/1513372
Participants
| Role | Name | HCID | Charge |
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| Reactant | L-Tartaric acid | HCID 444305 | — |
| Reactant | [4-(5-aminomethyl-2-fluorophenyl)piperidine-1-yl][7-fluoro-1-(2-methoxyethyl)-4-trifluoromethoxy-1H-indol-3-yl]methanone | HCID 44631896 | — |
| Solvent | Acetonitrile--water (1/1) | HCID 18373917 | — |
| Product | 2,3-Dihydroxybutanedioic Acid | HCID 875 | — |
Reaction Steps
[4-(5-aminomethyl-2-fluoro-phenyl)-piperidin-1-yl]-[7-fluoro-1-(2-methoxy-ethyl)-4-trifluoromethoxy-1H-indol-3-yl]-methanone (0.250 g, 0.554 mmol) was weighed in a 20 ml glass vial. A solution of L-(+)-tartaric acid at 2.66 mmol/ml in 5:1 (v/v) acetonitrile/water was prepared, and 0.2084 ml of this solution was added to the weighed solid with stirring and heating to ˜60° C. giving a clear solution. The solution was then evaporated in vacuo on a rotary evaporator leaving a glassy solid which was recrystallized in hot isopropyl acetate to which a minimum amount of isopropanol was added to give a clear solution. Upon cooling the crystalline product was isolated by filtration and dried in vacuo at room temperature.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08217178B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-6355bd97e5144dd4b713f75a552ad1ee |
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| Source note | uspto-grants-2012_07 |
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