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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2399886Generated: November 2, 2026

bis(4-methylbenzoyl) (2R,3R)-2,3-dihydroxybutanedioate → HCID 86748987, compound

https://huagongshe.com/reaction/2399886

Reaction equation

Participants

RoleNameHCIDCharge
Reactantbis(4-methylbenzoyl) (2R,3R)-2,3-dihydroxybutanedioateHCID 14721060—
SolventWaterHCID 962—
ProductHCID 86748987HCID 8674898758.6%

Reaction Conditions

Temperature75 °C

Reaction Steps

To a 300 ml reaction vessel equipped with a stirrer, thermometer, condenser and a dropping funnel, 50 g of O,O'-di-p-toluoyl-L-tartaric anhydride and 150 g of water were supplied and the mixture was stirred at 90°-95° C. for 1 hour to carry out hydrolysis. After cooling the reaction mixture to 75° C. 0 1 g of seed crystal of O,O'-di-p-toluoyl-L-tartaric acid was added and the mixture was slowly cooled. Since oily product began to crystalize at 73° C., the mixture was stirred for 1 hour at this temperature. After completion of crystallization, the reaction slurry was cooled to room temperature and the crystals were collected by filtration. The thus obtained cake was dried to obtain 32.3 g of O,O'-di-p-toluoyl-L-tartaric acid hydrate in the form of white crystals. The content of crystal water was measured by the Karl Fischer method, which was 4.9% (yield: 58.6%). The crystals were sieved through a 20-mesh sieve and 48 wt % of the crystals passed through the sieve. The amount of the crystals which adhered to the wall or to the stirrer of the reaction apparatus so that which could not be removed from the reaction apparatus was 20.9 g which was 39.3 wt % of the total crystals produced.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05451687
Source datasetuspto-grants-1995_09
ORD IDord-aa45ac1341bc46babd71a36fa0908490
Source noteuspto-grants-1995_09