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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734916Generated: November 2, 2026

2,3-Dihydroxybutanedioic Acid → HCID 53698866, compound

https://huagongshe.com/reaction/1734916

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dihydroxybutanedioic AcidHCID 875—
ReactantBoron trifluoride etherateHCID 8000—
ReactantDiisobutylaluminumhydrideHCID 21225700—
ReactantHCID 53716971HCID 53716971—
SolventDichloromethaneHCID 6344—
ProductHCID 53698866HCID 5369886689.5%

Reaction Steps

68 μl (0.60 mmol) of boron trifluoride etherate were added at -78° C. to a solution of 228 mg (0.5 mmol) of N-[2-isopropyl-6-(2-ethoxycarbonylethenyl)phenyl]-2-(9H-xanthen-9-yl)acetamide [prepared as described in step (i) above] in 6 ml of methylene chloride. The resulting mixture was stirred for 30 minutes, after which 2.0 ml of a 1.0M solution of diisobutylaluminum hydride were added dropwise over a period of 5 minutes. The temperature of the mixture was allowed to rise to room temperature, and then 10 ml of a 10% w/v aqueous solution of tartaric acid were added to the reaction mixture in order to stop the reaction. The reaction mixture was then diluted with methylene chloride. The diluted mixture was washed with a saturated aqueous solution of sodium hydrogencarbonate and then with a saturated aqueous solution of sodium chloride. The organic phase was dried over anhydrous sodium sulfate, and the solvent was removed by distillation under reduced pressure. The resulting residue was triturated with a mixture of diethyl ether and hexane to cause crystallization. The crystals were collected by filtration to give 185 mg (yield 85%) of the title alcohol derivative, melting at 225°-227° C. (after recrystallization from a mixture of acetonitrile and diisopropyl ether).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05534529
Source datasetuspto-grants-1996_07
ORD IDord-3065e7817b7c42c48473bc8c469f30a7
Source noteuspto-grants-1996_07