HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1460551Generated: November 4, 2026
2,3-Dihydroxybutanedioic Acid → HCID 88527765, compound
https://huagongshe.com/reaction/1460551
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,3-Dihydroxybutanedioic Acid | HCID 875 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 1,2,3,6-Tetrahydro-4-phenylpyridine | HCID 82553 | — |
| Reactant | HCID 4152550 | HCID 4152550 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 88527765 | HCID 88527765 | — |
Reaction Steps
20 mmol of 2-amino-5-(2-chloroethyl)-4-phenylthiazole and 20 mmol of 4-phenyl-1,2,3,6-tetrahydropyridine were thoroughly mixed and were heated under an N2 atmosphere at 120° C. until conversion was complete, which was the case after 20 minutes. After cooling, the solidified melt was stirred with water, the oily solid residue was separated off and stirred thoroughly with methanol and the solid was filtered off under suction. The filter residue was partitioned in 2 N NaOH/CH2Cl2 and the organic phase was separated off, dried and evaporated down. The residue was dissolved in methanol while hot, one equivalent of tartaric acid was added and the precipitated solid was filtered off under suction and purified by recrystallization from ethyl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05071864 |
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| Source dataset | uspto-grants-1991_12 |
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| ORD ID | ord-5aae88503a7249d39c480b52c37343cb |
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| Source note | uspto-grants-1991_12 |
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