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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1074650Generated: October 26, 2026

Water → (-)-1-Benzoyl-2,3-di-p-toluenesulfonyl glycerol

https://huagongshe.com/reaction/1074650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChloroformHCID 6212—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant1-MonobenzoylglycerolHCID 137911—
SolventPyridineHCID 1049—
Product(-)-1-Benzoyl-2,3-di-p-toluenesulfonyl glycerolHCID 1291408672%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 35.5 g (181 mmol) of (-)-1-benzoyl glycerol (G) in 250 ml of dry pyridine at 0° C. is added 83 g (433 mmol) of p-toluenesulfonyl chloride. The mixture is stirred at 0° C. for 15 minutes and then stored in a refrigerator for 144 hours. After cooling the reaction mixture to 0° C., 10 ml of water are added, the mixture is stirred for 10 minutes, and then poured into excess water. The aqueous solution is separated from the gummy product, and extracted with chloroform. The gummy residue is dissolved in chloroform and the combined chloroform solution is washed sequentially with 3 N hydrochloric acid, water, 5% sodium bicarbonate solution, and water. The chloroform solution is dried over Na2SO4 and concentrated under reduced pressure to obtain a solid which, upon recrystallization from absolute ethanol, gives 65.5 g (130 mmol, 72%) of (-)-1-benzoyl-2,3-di-p-toluenesulfonyl glycerol (see Formula (H) in Scheme 2), m.p. 105°-106° C. [α]D2° -22.7 (c, 5.92, CHCl3). 1H NMR (CDCl3) δ8-7 (m, 13H); 4.9 (m, 1H); 4.45 (d, 2H, J=6 Hz); 4.35 (d, 2H, J=5 Hz); 2.42 (s, 3H); 2.38 (s, 3H). 13C NMR (CDCl3) 165.162, 145.136, 133.108, 132.466, 131.649, 129.430, 128.671, 128.087, 127.678, 75.306, 66.899, 61.994, 21.591 ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04393240
Source datasetuspto-grants-1983_07
ORD IDord-8ffdabc5f56d4d86a9f7b99d1f9f11ce
Source noteuspto-grants-1983_07